510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K010317Substantially Equivalent

Av 800 Ventilator

Penlon, Ltd., Oxfordshire, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K010317 is the FDA 510(k) clearance record for AV 800 VENTILATOR, a class II device, cleared for Penlon , Ltd. on under FDA product code CBK (Ventilator, Continuous, Facility Use). FDA records list 22 510(k) clearances for Penlon , Ltd., from to . As of , FDA records show no recalls naming K010317.

Clearance record

Decision date
Received
(171 days to decision)
Product code
CBK Ventilator, Continuous, Facility Use
Regulation
21 CFR 868.5895
Device class
Class II
Review panel
Anesthesiology
Applicant
Penlon , Ltd. Radley Rd., Oxfordshire, GB
510(k) summary
Summary
Third party review
No

Clearances, product code CBK

Trailing 12 months
4 clearances under product code CBK in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CBK, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20261
April 20261
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260