510(k) Report

510(k) · Cleared

Cleared

Sterile Hypodermic Syringes for Single Use with Safety Needles

K221073510(k) TraditionalCleared Oct 4, 2022175-day reviewClass II21 CFR 880.5860

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

Sichuan Prius Biotechnology Co., Ltd. · MEG Syringe, Antistick

Cleared on Oct 4, 2022 as substantially equivalent to K193526 (Jiangsu Caina Medical Co.,Ltd, 2020) after a 175-day review. Its family tree reaches back 8 generations to 1977.

Decided
Oct 4, 2022
Review
175 days
Class
Class II
Product code
MEG
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K771205 (1977). 19 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 8 generations backK771205 Hypodermic SyringeTerumo America, Inc. · 1977
  2. 7 generations backK980181 Terumo Disposable Hypodermc SyringeTerumo Medical Corp. · 1998 · Recalled
  3. 6 generations backK023271 Terumo Syringe with/Without NeedleTerumo Medical Corp. · 2002
  4. 5 generations backK052034 Terumo Syringe with/Without NeedleTerumo Medical Corp. · 2005
  5. 4 generations backK063613 Modification to Terumo Syringe with/Without NeedleTerumo Medical Corp. · 2006
  6. 3 generations backK083514 Terumo Syringe with/Without NeedleTerumo Europe N.V. · 2009
  7. 2 generations backK170651 Sterile Disposable Syringe with Safety Needle, Sterile Disposable…Yangzhou Medline Industry, Co., Ltd. · 2017
  8. 1 generation backK193526 Syringe with safety needle, Safety needleJiangsu Caina Medical Co.,Ltd · 2020
  9. This deviceK221073 Sterile Hypodermic Syringes for Single Use with Safety NeedlesSichuan Prius Biotechnology Co., Ltd. · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K771205Hypodermic SyringeTerumo America, Inc.1977—
−7K980181Terumo Disposable Hypodermc SyringeTerumo Medical Corp.19981
−6K023271Terumo Syringe with/Without NeedleTerumo Medical Corp.2002—
−5K052034Terumo Syringe with/Without NeedleTerumo Medical Corp.2005—
−4K063613Modification to Terumo Syringe with/Without NeedleTerumo Medical Corp.2006—
−3K083514Terumo Syringe with/Without NeedleTerumo Europe N.V.2009—
−2K170651Sterile Disposable Syringe with Safety Needle, Sterile Disposable Syringe with…Yangzhou Medline Industry, Co., Ltd.2017—
−1K193526Syringe with safety needle, Safety needleJiangsu Caina Medical Co.,Ltd2020—
0 (this device)K221073Sterile Hypodermic Syringes for Single Use with Safety NeedlesSichuan Prius Biotechnology Co., Ltd.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197710
199010
199310
199810
200110
200310
200410
200510
200610
200710
201210
FIG. 1 — Lineage of K221073, 1977–2022Source: 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 MEG? 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 MEG device

  1. #1 K192551 1ml Luer Slip or Luer Lock Syringe, Syringe…score 19.6 · 7 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
*K193526Syringe with safety needle, Safety needle
Summary page 5
…II; Product Code: FMI; Regulation Number: 21CFR 880.5570; Review Panel: General Hospital; 5. Identification of Predicate Device 510(k) Number: K193526 Product Name: Syringe with Safety Needle 6. Device Description The Sterile Hypodermic Syringes for Single Use wit…
Jiangsu Caina Medical Co.,Ltd2020—

Also cleared against K193526: 3 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 45 years and passes through 6 companies; a new generation was cleared every 3.0 years on median.
  • 4 of the 19 ancestors have a recall of any class.
  • 3 other devices also cite its predicate K193526.

How does its category compare?

All MEG devices

MEG Syringe, Antistick: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · MEG

1in 2025

2007: 82008: 42009: 22010: 22011: 52012: 52013: 12014: 52015: 72016: 32017: 32018: 12019: 42020: 42021: 52022: 132023: 52025: 12026 (partial year): 1
2007high 13 (2022) · low 0 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MEG

229in 2023

2007: 100 days median2008: 145 days median2011: 113 days median2012: 109 days median2014: 153 days median2015: 253 days median2016: 179 days median2017: 130 days median2019: 249 days median2020: 296 days median2021: 152 days median2022: 216 days median2023: 229 days median
2007high 296 (2020) · low 100 (2007)2026

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

Recalls per year · MEG

1in 2024

2008: 12010: 12013: 52015: 12024: 1, 1 Class I
2007high 5 (2013) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · MEG

148in 2025

2007: 212008: 202009: 262010: 342011: 342012: 222013: 272014: 362015: 512016: 942017: 1812018: 2692019: 4972020: 3532021: 5412022: 1702023: 1202024: 1122025: 148
2007high 541 (2021) · low 20 (2008)2025

MAUDE reports naming product code MEG, 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
20078100021
20084145120
20092—026
20102—134
20115113034
20125109022
20131—527
20145153036
20157253151
20163179094
201731300181
20181—0269
201942490497
202042960353
202151520541
2022132160170
202352290120
20240—1 (1)112
20251—0148
20261—0—

What is it indicated for?

The Sterile Hypodermic Syringes for Single Use with Safety Needles is intended for use in the aspiration and injection of fluids for medical purpose. After withdrawal of the needle from the body, the attached needle safety shield can be manually activated to cover the needle immediately after use to minimize risk of accidental needlesticks.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K221073: Sterile Hypodermic Syringes for Single Use with Safety Needles.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K221073

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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