510(k) Report

510(k) · Cleared

Cleared

PB 7200 Series Ventilatory System W/Keyboard

K930017510(k) TraditionalCleared Sep 22, 1994626-day reviewClass II21 CFR 868.5895

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

Puritan Bennett Corp. · CBK Ventilator, Continuous, Facility Use

Cleared on Sep 22, 1994 after a 626-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 44 of the 137 devices in its family, counting itself, have a Class I recall. 136 later devices descend from it.

Decided
Sep 22, 1994
Review
626 days
Class
Class II
Product code
CBK
Recalls
None
Predicates
0

136 later devices descend from it, 2 citing it directly. 44 of the 137 devices in this family, counting this one, have a Class I recall.

Descendants, by year cleared 2003: 1 descendant cleared, 1 with a Class I recall12007: 4 descendants cleared, 2 with a Class I recall22004: 5 descendants cleared, 1 with a Class I recall12005: 7 descendants cleared2017: 7 descendants cleared, 4 with a Class I recall42008: 8 descendants cleared, 2 with a Class I recall22010: 7 descendants cleared, 1 with a Class I recall12009: 8 descendants cleared, 2 with a Class I recall22006: 4 descendants cleared2026: 3 descendants cleared2012: 15 descendants cleared, 6 with a Class I recall62014: 5 descendants cleared, 1 with a Class I recall12011: 13 descendants cleared, 7 with a Class I recall72021: 5 descendants cleared, 2 with a Class I recall22015: 7 descendants cleared, 1 with a Class I recall12016: 7 descendants cleared, 3 with a Class I recall32019: 6 descendants cleared, 3 with a Class I recall32013: 10 descendants cleared, 4 with a Class I recall42024: 5 descendants cleared2018: 3 descendants cleared, 1 with a Class I recall12025: 2 descendants cleared2023: 1 descendant cleared, 1 with a Class I recall12020: 3 descendants cleared, 2 with a Class I recall21990200020102020
  1. This deviceK930017 PB 7200 Series Ventilatory System W/KeyboardPuritan Bennett Corp. · 1994
  2. Descendant · cites it directly · 134 of its ownK023366 Datex-Ohmeda 7900 Ventilator EnhancementsDatex-Ohmeda, Inc. · 2003 · Recalled (Class I)
  3. Descendant · 2 generations on · 107 of its ownK041775 GE Datex-Ohmeda Engstrom CarestationDatex-Ohmeda, Inc. · 2004
  4. Descendant · 3 generations on · 57 of its ownK051767 LTV 1000 VentilatorPulmonetic Systems, Inc. · 2005
  5. Descendant · 3 generations on · 49 of its ownK051895 GE Datex-Ohmeda Engstrom CarestationDatex-Ohmeda, Inc. · 2005
  6. Descendant · 4 generations on · 48 of its ownK060862 GE Datex-Ohmeda Engstrom CarestationDatex-Ohmeda, Inc. · 2006 · Recalled

Showing 5 of 136 descendants. See all descendants

Descendants cleared per year

2003: 12004: 52005: 72006: 42007: 42008: 82009: 82010: 72011: 132012: 152013: 102014: 52015: 72016: 72017: 72018: 32019: 62020: 32021: 52023: 12024: 52025: 22026: 3
2003high 15 (2012) · low 0 (2022)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 136 · See all
  • K023366Datex-Ohmeda 7900 Ventilator EnhancementsDatex-Ohmeda, Inc. · 2003 · cites it directly134descendants
  • K041775GE Datex-Ohmeda Engstrom CarestationDatex-Ohmeda, Inc. · 2004 · 2 generations on107descendants
  • K051767LTV 1000 VentilatorPulmonetic Systems, Inc. · 2005 · 3 generations on57descendants
  • K051895GE Datex-Ohmeda Engstrom CarestationDatex-Ohmeda, Inc. · 2005 · 3 generations on49descendants
  • K060862GE Datex-Ohmeda Engstrom CarestationDatex-Ohmeda, Inc. · 2006 · 4 generations on48descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K930017PB 7200 Series Ventilatory System W/KeyboardPuritan Bennett Corp.1994—
+1K023366Datex-Ohmeda 7900 Ventilator EnhancementsDatex-Ohmeda, Inc.2003Class I
+2K041775GE Datex-Ohmeda Engstrom CarestationDatex-Ohmeda, Inc.2004—
+3K051767LTV 1000 VentilatorPulmonetic Systems, Inc.2005—
+3K051895GE Datex-Ohmeda Engstrom CarestationDatex-Ohmeda, Inc.2005—
+4K060862GE Datex-Ohmeda Engstrom CarestationDatex-Ohmeda, Inc.20061

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200311
200451
200570
200640
200742
200882
200982
201071
2011137
2012156
2013104
201451
201571
201673
201774
201831
201963
202032
202152
202311
202450
202520
202630
FIG. 1 — Lineage of K930017, 1994–2026Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

44 devices in this family have a Class I recall. 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 CBK device

  1. #1 K252663 Inbentus Versatilescore 16.0 · 17 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?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (136)

See all 136

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K023366Datex-Ohmeda 7900 Ventilator Enhancements Class IDatex-Ohmeda, Inc.2003134
K063650Ventilator with Respiratory Mechanics, Model 840Puritan Bennett Corp.20070

Has anything in its family been recalled? (44 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K023366Datex-Ohmeda 7900 Ventilator EnhancementsDatex-Ohmeda, Inc. · 2003 · Cites it directly · ◆ in the 2003 descendants bar of FIG. 11 Class I recall
  • K172045Aestiva 7900, Aestiva MRI, Aestiva 7100, Aestiva 7100 Compact, Aespire 100, Aespire 7100, Aespire 7900…Datex-Ohmeda, Inc. · 2017 · 2 generations on · ◆ in the 2017 descendants bar of FIG. 110 Class I recalls
  • K042419Fabius GS/Fabius Tiro Anesthesia SystemDraeger Medical, Inc. · 2004 · 2 generations on · ◆ in the 2004 descendants bar of FIG. 14 Class I recalls
  • K072884Fabius MriDraeger Medical AG & Co. KG · 2008 · 3 generations on · ◆ in the 2008 descendants bar of FIG. 11 Class I recall
  • K090888Newport HT70 Family of VentilatorsNewport Medical Instruments, Inc. · 2009 · 4 generations on · ◆ in the 2009 descendants bar of FIG. 13 Class I recalls
  • K083526Trilogy 100 VentilatorRespironics Inc., Sleep & Home Respiratory Group · 2009 · 4 generations on · ◆ in the 2009 descendants bar of FIG. 15 Class I recalls
  • K070899Puritan Bennett Legendair XL2Nellcor Puritan Bennett · 2007 · 4 generations on · ◆ in the 2007 descendants bar of FIG. 11 Class I recall
  • K122445Aespire 7900, Aespire ViewDatex-Ohmeda · 2012 · 4 generations on · ◆ in the 2012 descendants bar of FIG. 11 Class I recall
  • K070594Palmtop Ventilator, Models PTV-8, PTV-10Pulmonetic Systems, Inc. · 2007 · 5 generations on · ◆ in the 2007 descendants bar of FIG. 12 Class I recalls
  • K111146Newport HT70 VentilatorNewport Medical Instruments, Inc. · 2011 · 5 generations on · ◆ in the 2011 descendants bar of FIG. 14 Class I recalls
  • K081521Modification to Hamilton-G5Hamilton Medical AG · 2008 · 5 generations on · ◆ in the 2008 descendants bar of FIG. 11 Class I recall
  • K102471AS3700 Anesthsia Delivery SystemMindray DS USA, Inc. · 2011 · 5 generations on · ◆ in the 2011 descendants bar of FIG. 12 Class I recalls

Nearest 12 of 44 shown.

What does this lineage say?

  • Of its descendants, K023366 (Datex-Ohmeda, Inc., 2003) has gone furthest, with 134 descendants of its own.

How does its category compare?

All CBK devices

CBK Ventilator, Continuous, Facility Use: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · CBK

4in 2025

2007: 112008: 182009: 122010: 142011: 132012: 172013: 52014: 52015: 72016: 42017: 62018: 42019: 82020: 52021: 62023: 52024: 92025: 42026 (partial year): 3
2007high 18 (2008) · low 0 (2022)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CBK

163in 2025

2007: 142 days median2008: 115 days median2009: 122 days median2010: 150 days median2011: 192 days median2012: 207 days median2013: 277 days median2014: 439 days median2015: 266 days median2016: 323 days median2017: 280 days median2018: 183 days median2019: 435 days median2020: 176 days median2021: 267 days median2023: 309 days median2024: 203 days median2025: 163 days median2026 (partial year): 235 days median
2007high 439 (2014) · low 115 (2008)2026

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

Recalls per year · CBK

14in 2024

2007: 172008: 232009: 82010: 92011: 122012: 2, 1 Class I2013: 5, 2 Class I2014: 5, 4 Class I2015: 6, 4 Class I2016: 4, 1 Class I2017: 12018: 3, 3 Class I2019: 14, 13 Class I2020: 42021: 21, 19 Class I2022: 8, 4 Class I2023: 4, 3 Class I2024: 14, 14 Class I2026 (partial year): 15, 13 Class I
2007high 23 (2008) · low 0 (2025)2026

Class I (81 since 2007) Class II/III not classified

Adverse event reports per year · CBK

13,991in 2025

2007: 1,5312008: 1,9332009: 1,7662010: 1,7992011: 1,8772012: 5,5092013: 7,9212014: 7,6002015: 11,8762016: 16,0562017: 14,4512018: 9,8492019: 9,1002020: 11,0962021: 13,3222022: 15,9742023: 24,9282024: 20,3362025: 13,991
2007high 24,928 (2023) · low 1,531 (2007)2025

MAUDE reports naming product code CBK, 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
200711142171,531
200818115231,933
20091212281,766
20101415091,799
201113192121,877
2012172072 (1)5,509
201352775 (2)7,921
201454395 (4)7,600
201572666 (4)11,876
201643234 (1)16,056
20176280114,451
201841833 (3)9,849
2019843514 (13)9,100
20205176411,096
2021626721 (19)13,322
20220—8 (4)15,974
202353094 (3)24,928
2024920314 (14)20,336
20254163013,991
2026323515 (13)—
Cite this page

510(k) Report. “K930017: PB 7200 Series Ventilatory System W/Keyboard.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K930017

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026