510(k) Report

510(k) · Cleared

Cleared

Sevoflurane Vaporizer Adaptor

K110608510(k) TraditionalCleared Jul 20, 2011139-day reviewClass II21 CFR 868.5880

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

Piramal Critcal Care, Inc (Formerly Minrad, Inc) · CAD Vaporizer, Anesthesia, Non-Heated

Cleared on Jul 20, 2011 as substantially equivalent to K053564 (Penlon Limited, 2006) after a 139-day review. Its family tree reaches back 2 generations to 1995.

Decided
Jul 20, 2011
Review
139 days
Class
Class II
Product code
CAD
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K945993 (1995). No later device cites it as a predicate yet.

  1. Root · 2 generations backK945993 VapofilSouthmedic, Inc. · 1995 · Recalled
  2. 1 generation backK053564 Keyed Filler Bottle Adaptor, Models 53450, 53452, 53453, 53454Penlon Limited · 2006
  3. This deviceK110608 Sevoflurane Vaporizer AdaptorPiramal Critcal Care, Inc (Formerly Minrad, Inc) · 2011
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K945993VapofilSouthmedic, Inc.19952
−1K053564Keyed Filler Bottle Adaptor, Models 53450, 53452, 53453, 53454Penlon Limited2006—
0 (this device)K110608Sevoflurane Vaporizer AdaptorPiramal Critcal Care, Inc (Formerly Minrad, Inc)2011—
FIG. 1 — Lineage of K110608, 1995–2011Source: 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 CAD? 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 CAD device

  1. #1 K240375 V80 Anesthetic Vaporizer (V80)score 8.9 · 3 generations · no Class I recall
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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
*K053564Keyed Filler Bottle Adaptor, Models 53450, 53452, 53453, 53454
Summary page 1
…illing Adaptor Classification: Anesthetic Vaporizer (21 CFR 868.5880, Product Code CAD) Predicate Device: Keyed Filler Bottle Adaptor (K053564) Description of Device: The Sevoflurane Vaporizer Adaptor will fit securely to the bottle and the…
Penlon Limited2006—

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 16 years and passes through 3 companies; a new generation was cleared every 11.0 years on median.
  • 1 of the 2 ancestors has a recall of any class.

How does its category compare?

All CAD devices

CAD Vaporizer, Anesthesia, Non-Heated: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · CAD

1in 2024

2011: 12015: 12018: 12024: 1
2007high 1 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CAD

Too few CAD 510(k)s in any year since 2007 to give a median.

Recalls per year · CAD

2in 2025

2024: 52025: 2, 2 Class I
2007high 5 (2024) · low 0 (2007)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · CAD

2,678in 2025

2007: 302008: 292009: 392010: 322011: 412012: 142013: 122014: 52015: 412016: 92017: 142018: 112019: 122020: 112021: 122022: 132023: 442024: 2552025: 2,678
2007high 2,678 (2025) · low 5 (2014)2025

MAUDE reports naming product code CAD, 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
20070—030
20080—029
20090—039
20100—032
20111—041
20120—014
20130—012
20140—05
20151—041
20160—09
20170—014
20181—011
20190—012
20200—011
20210—012
20220—013
20230—044
20241—5255
20250—2 (2)2,678
20260—0—

What is it indicated for?

The Sevoflurane Vaporizer Adaptor is intended to be used by qualified personnel as a means of filling Sevoflurane from a Piramal Sevoflurane bottle into a user-owned QuikFil Sevoflurane vaporizer.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K110608: Sevoflurane Vaporizer Adaptor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K110608

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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