510(k) Report

510(k) · Cleared

Recalled · 2010

Cryocare CS Surgical System

K060279510(k) SpecialCleared Feb 28, 200626-day reviewClass II21 CFR 878.4350Recalls 3

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Endocare, Inc. · GEH Unit, Cryosurgical, Accessories

Cleared on Feb 28, 2006 as substantially equivalent to K050347 (Endocare, Inc., 2005) after a 26-day review. Its family tree reaches back 6 generations to 1993. 9 later devices descend from it. It has been recalled 3 times.

Decided
Feb 28, 2006
Review
26 days
Class
Class II
Product code
GEH
Recalls
3
Predicates
1

Its longest line of descent runs back 6 generations to K926514 (1993). 17 ancestors in all, the oldest K850478 (1985). 9 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2004: 1 other ancestor2002: 2 other ancestors2000: 1 other ancestor2001: 1 other ancestor1999: 2 other ancestors1997: 1 other ancestor1986: 1 other ancestor1985: 1 other ancestor1994: 1 other ancestor2010: 1 descendant cleared2015: 2 descendants cleared2016: 1 descendant cleared2020: 1 descendant cleared2023: 2 descendants cleared2025: 2 descendants clearedK926514 · Endoscopic Ultrasound System Type 20 · Olympus Corp. · 1993 · recalledK963023 · Ultrasound Gastroscope GF Type UM30P · Olympus America, Inc. · 1997K994373 · Hdi 1500/SA 8800 Ultrasound System with Multiplane Transesophageal Ultrasound Transducer (MTP7-4) · Atl Ultrasound, Inc. · 2000K030191 · Terason Model 2000/Bas Portable Ultrasound System · Teratech Corp. · 2003K032333 · Cryocare CS Surgical System · Endocare, Inc. · 2003K050347 · Modification to Cryocare CS Surgical System · Endocare, Inc. · 20051990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 2 other ancestors4 generations back: 3 other ancestors5 generations back: 4 other ancestors6 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 1 descendant3 generations forward: 2 descendants4 generations forward: 1 descendant5 generations forward: 4 descendants K050347 · Modification to Cryocare CS Surgical System · Endocare, Inc. · 2005K032333 · Cryocare CS Surgical System · Endocare, Inc. · 2003K030191 · Terason Model 2000/Bas Portable Ultrasound System · Teratech Corp. · 2003K994373 · Hdi 1500/SA 8800 Ultrasound System with Multiplane Transesophageal Ultrasound Transducer (MTP7-4) · Atl Ultrasound, Inc. · 2000K963023 · Ultrasound Gastroscope GF Type UM30P · Olympus America, Inc. · 1997K926514 · Endoscopic Ultrasound System Type 20 · Olympus Corp. · 1993 · recalled−50+5
  1. Root · 6 generations backK926514 Endoscopic Ultrasound System Type 20Olympus Corp. · 1993 · Recalled
  2. 5 generations backK963023 Ultrasound Gastroscope GF Type UM30POlympus America, Inc. · 1997
  3. 4 generations backK994373 Hdi 1500/SA 8800 Ultrasound System with Multiplane Transesophageal…Atl Ultrasound, Inc. · 2000
  4. 3 generations backK030191 Terason Model 2000/Bas Portable Ultrasound SystemTeratech Corp. · 2003
  5. 2 generations backK032333 Cryocare CS Surgical SystemEndocare, Inc. · 2003
  6. 1 generation backK050347 Modification to Cryocare CS Surgical SystemEndocare, Inc. · 2005
  7. This deviceK060279 Cryocare CS Surgical SystemEndocare, Inc. · 2006
  8. Descendant · cites it directly · 8 of its ownK101333 Cryocare CS Surgical SystemEndocare, Inc. · 2010 · Recalled
  9. Descendant · 2 generations on · 7 of its ownK141110 Cryocare CS Surgical SystemHealthtronics · 2015
  10. Descendant · 3 generations on · 6 of its ownK151968 Cryocare CS-3 Surgical System version 5Healthtronics · 2015
  11. Descendant · 3 generations on · 5 of its ownK153489 Cryocare CS Surgical SystemHealthtronics · 2016
  12. Descendant · 4 generations on · 4 of its ownK201588 CRYOCARE TOUCH System and Accessories, Endocare 1.7mm Round Ice…Varian Medical Systems, Inc. · 2020

Showing 5 of 9 descendants. See all descendants

Descendants cleared per year

2010: 12015: 22016: 12020: 12023: 22025: 2
2010high 2 (2015) · low 0 (2011)2026

Most influential descendants

Showing 5 of 9 · See all
  • K101333Cryocare CS Surgical SystemEndocare, Inc. · 2010 · cites it directly8descendants
  • K141110Cryocare CS Surgical SystemHealthtronics · 2015 · 2 generations on7descendants
  • K151968Cryocare CS-3 Surgical System version 5Healthtronics · 2015 · 3 generations on6descendants
  • K153489Cryocare CS Surgical SystemHealthtronics · 2016 · 3 generations on5descendants
  • K201588CRYOCARE TOUCH System and Accessories, Endocare 1.7mm Round Ice PerCryo Cryoprobe…Varian Medical Systems, Inc. · 2020 · 4 generations on4descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K926514Endoscopic Ultrasound System Type 20Olympus Corp.19931
−5K963023Ultrasound Gastroscope GF Type UM30POlympus America, Inc.1997—
−4K994373Hdi 1500/SA 8800 Ultrasound System with Multiplane Transesophageal Ultrasound…Atl Ultrasound, Inc.2000—
−3K030191Terason Model 2000/Bas Portable Ultrasound SystemTeratech Corp.2003—
−2K032333Cryocare CS Surgical SystemEndocare, Inc.2003—
−1K050347Modification to Cryocare CS Surgical SystemEndocare, Inc.2005—
0 (this device)K060279Cryocare CS Surgical SystemEndocare, Inc.2006—
+1K101333Cryocare CS Surgical SystemEndocare, Inc.20102
+2K141110Cryocare CS Surgical SystemHealthtronics2015—
+3K151968Cryocare CS-3 Surgical System version 5Healthtronics2015—
+3K153489Cryocare CS Surgical SystemHealthtronics2016—
+4K201588CRYOCARE TOUCH System and Accessories, Endocare 1.7mm Round Ice PerCryo…Varian Medical Systems, Inc.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198510
198610
199410
199710
199920
200010
200110
200220
200410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201010
201520
201610
202010
202320
202520
FIG. 1 — Lineage of K060279, 1993–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in GEH? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new GEH device

  1. #1 K211099 Freeze’n Clear Skin Clinic Warts & Tagsscore 25.4 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K050347Modification to Cryocare CS Surgical System
Summary page 1
…marketed by Endocare: Manufacturer Device Name 510-K Number Decision Date Endocare, Inc. Cryocare CSTM K050347 February 05, 2005 * Device Description: The Cryocare CS Surgical System consists of a compact, easy-to-opera…
Endocare, Inc.2005—

Also cleared against K050347: 1 other device →

What descends from it? (9)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K101333Cryocare CS Surgical SystemEndocare, Inc.20108

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Nov 4, 2010Not classifiedZ-0615-2011OtherMislabeled : The label on the outer box and inner pouch of the EndoCare 2.4mm CryoProbe (CRYO-44F) inaccurately reference the CVA2400 (2.4mm Variable Probe aka: V-Probe).
Dec 5, 2008Not classifiedZ-1401-2010OtherEndocare received a report of a patient death that occurred during a prostate cryoablation procedure. An autopsy attributed the cause of death to an air embolism. The safety notice for the cryoprobes was issued to refocus attention on the…
Dec 5, 2008Not classifiedZ-1400-2010OtherEndocare received a report of a patient death that occurred during a prostate cryoablation procedure. An autopsy attributed the cause of death to an air embolism. The safety notice for the cryoprobes was issued to refocus attention on the…

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 13 years and passes through 5 companies; a new generation was cleared every 2.9 years on median.
  • 4 of the 17 ancestors have a recall of any class.
  • Of its descendants, K101333 (Endocare, Inc., 2010) has gone furthest, with 8 descendants of its own.
  • 1 other device also cites its predicate K050347.

How does its category compare?

All GEH devices

GEH Unit, Cryosurgical, Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GEH

10in 2025

2007: 62008: 12009: 42010: 42011: 72012: 42013: 42014: 62015: 112016: 152017: 122018: 62019: 62020: 82021: 62022: 62023: 82024: 92025: 102026 (partial year): 8
2007high 15 (2016) · low 1 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GEH

77in 2025

2007: 71 days median2009: 121 days median2010: 86 days median2011: 91 days median2012: 96 days median2013: 76 days median2014: 42 days median2015: 72 days median2016: 60 days median2017: 83 days median2018: 42 days median2019: 115 days median2020: 113 days median2021: 206 days median2022: 56 days median2023: 136 days median2024: 85 days median2025: 77 days median2026 (partial year): 148 days median
2007high 206 (2021) · low 42 (2014)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · GEH

2in 2023

2007: 32008: 22009: 132010: 42012: 32014: 22018: 12019: 12020: 372023: 22026 (partial year): 2
2007high 37 (2020) · low 0 (2011)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · GEH

171in 2025

2007: 232008: 292009: 212010: 1732011: 612012: 912013: 912014: 572015: 972016: 1432017: 2162018: 2082019: 4552020: 2772021: 2132022: 2302023: 1642024: 1412025: 171
2007high 455 (2019) · low 21 (2009)2025

MAUDE reports naming product code GEH, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007671323
20081—229
200941211321
20104864173
2011791061
2012496391
2013476091
2014642257
20151172097
201615600143
201712830216
20186421208
201961151455
2020811337277
202162060213
20226560230
202381362164
20249850141
202510770171
202681482—

What is it indicated for?

The Cryocare CS Surgical System is intended for use in open, minimally invasive or endoscopic surgical procedures in the areas in general surgery, urology, gynecology, oncology, neurology, dermatology, ENT, proctology, pulmonary surgery and thoracic surgery. The system is designed to freeze/ablate tissue by the application of extreme cold temperatures including prostate and kidney tissue, liver metastases, tumors, skin lesions, and warts. In addition…

Read the full statement (140 words)

The Cryocare CS Surgical System is intended for use in open, minimally invasive or endoscopic surgical procedures in the areas in general surgery, urology, gynecology, oncology, neurology, dermatology, ENT, proctology, pulmonary surgery and thoracic surgery. The system is designed to freeze/ablate tissue by the application of extreme cold temperatures including prostate and kidney tissue, liver metastases, tumors, skin lesions, and warts.

In addition, the system is intended for use in the following indications:

General Surgery

* Destruction of warts or lesions

* Palliation of tumors of the oral cavity, rectum and skin

* Ablation of leukoplakia of the mouth, angiomas, sebaceous hyperplasia, basal cell tumors of the eyelid or canthus area, ulcerated basal cell tumors, dermatofibromas, small hemanglomas, mucocele cysts, multiple warts, plantar warts, hemorrhoids, anal fissures, perianal condylomata, pilonidal cysts, actinic and seborrheic keratoses, cavernous hemanglomas, recurrent cancerous lesions

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K060279: Cryocare CS Surgical System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K060279

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026