510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K051666Substantially Equivalent

Gav - General Anaesthetic Vaporizer

General Anaesthetic Services Limited, Keighley, West Yorkshire, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K051666 is the FDA 510(k) clearance record for GAV - GENERAL ANAESTHETIC VAPORIZER, a class II device, cleared for General Anaesthetic Services Limited on under FDA product code CAD (Vaporizer, Anesthesia, Non-Heated). FDA records list one 510(k) clearance for General Anaesthetic Services Limited. As of , FDA records show no recalls naming K051666.

Clearance record

Decision date
Received
(62 days to decision)
Product code
CAD Vaporizer, Anesthesia, Non-Heated
Regulation
21 CFR 868.5880
Device class
Class II
Review panel
Anesthesiology
Applicant
General Anaesthetic Services Limited Ingrow Bridge Business Park, Keighley, West Yorkshire, GB
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code CAD

Trailing 12 months

FDA records hold no clearances under product code CAD in the trailing twelve months.

FDA records show no clearances under product code CAD in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CAD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260