510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K844008Substantially Equivalent

Penlon Am1000 Anaesthesia Machine

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

K844008 is the FDA 510(k) clearance record for PENLON AM1000 ANAESTHESIA MACHINE, a class II device, cleared for Penlon, Inc. on under FDA product code BSZ (Gas-Machine, Anesthesia). FDA records list 22 510(k) clearances for Penlon, Inc., from to . As of , FDA records show no recalls naming K844008.

Clearance record

Decision date
Received
(151 days to decision)
Product code
BSZ Gas-Machine, Anesthesia
Regulation
21 CFR 868.5160
Device class
Class II
Review panel
Anesthesiology
Applicant
Penlon, Inc. Abingdon Ox 14 3ph, Abingdon Ox, GB
Third party review
No

Clearances, product code BSZ

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