PMS ANGIO DRAPE— 510(k) K890471

Substantially Equivalent

Professional Medical Services

FDA 510(k) clearance K890471 for PMS ANGIO DRAPE, Substantially Equivalent on 1989-02-27. Applicant: Professional Medical Services. Device class: 2.

Clearance details

Applicant: Professional Medical Services
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1989-01-31
Decision date: 1989-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Salt Lake, UT, US

Download summary PDF View on FDA.gov ↗

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More clearances from Professional Medical Services

K913094 — DISPOSABLE SLIDE VALVE MANIFOLD1992-01-27
K910378 — PRESSURE MONITORING EXTENSION LINE1991-04-22
K904508 — CONDOR ANALOG INFLATION SYRINGE1991-04-02
K904954 — CONDOR DIGITAL INFLATION SYRINGE1991-01-16
K902606 — RADIOPAQUE RULER1990-09-27

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