510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K030939Substantially Equivalent

Philips Compurecord Peri-Operative Information System Software

Philips North America LLC, Pittsburgh PA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K030939 is the FDA 510(k) clearance record for PHILIPS COMPURECORD PERI-OPERATIVE INFORMATION SYSTEM SOFTWARE, a class II device, cleared for Philips Medical Systems on under FDA product code BSZ (Gas-Machine, Anesthesia). FDA records list 680 510(k) clearances for Philips North America LLC, from to . As of , FDA records show no recalls naming K030939.

Clearance record

Decision date
Received
(112 days to decision)
Product code
BSZ Gas-Machine, Anesthesia
Regulation
21 CFR 868.5160
Device class
Class II
Review panel
Anesthesiology
Applicant
Philips Medical Systems 1082 Bower Hill Rd., Pittsburgh PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code BSZ

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