510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K792457Substantially Equivalent

Compressor

Pneupac, Ltd., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K792457 is the FDA 510(k) clearance record for COMPRESSOR, a class II device, cleared for Pneupac , Ltd. on under FDA product code BTI (Compressor, Air, Portable). FDA records list 20 510(k) clearances for Pneupac , Ltd., from to . As of , FDA records show no recalls naming K792457.

Clearance record

Decision date
Received
(64 days to decision)
Product code
BTI Compressor, Air, Portable
Regulation
21 CFR 868.6250
Device class
Class II
Review panel
Anesthesiology
Applicant
Pneupac , Ltd. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code BTI

Trailing 12 months

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

FDA records show no clearances under product code BTI in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BTI, 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