CARDIO-PAK LAPAROTOMY PACK— 510(k) K923233

Unknown

Cardio-Med-Associates, Inc.

FDA 510(k) clearance K923233 for CARDIO-PAK LAPAROTOMY PACK, Unknown on 1993-03-20. Applicant: Cardio-Med-Associates, Inc.. Device class: 2.

Clearance details

Applicant: Cardio-Med-Associates, Inc.
Product code: Code FZH
Device class: Class 2
Regulation: 21 CFR 878.5070
Advisory panel: General, Plastic Surgery
Date received: 1992-07-01
Decision date: 1993-03-20
Decision: Unknown
Clearance type: Traditional
Location: Billings, MT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FZH

K875305 — MODEL UCA / SPEC SYSTEM UCA1988-01-27
K871901 — ULTRAFLOW1987-06-01
K770084 — OPERATING ROOM VENTILATOR1977-02-23

More clearances from Cardio-Med-Associates, Inc.

K923231 — CARDIO-PAK BASIC PUMP PACK1993-07-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.