PROCEDURE & RECOVERY PATIENT SUIT— 510(k) K803171

Name: FDA 510(k) clearance K803171
Creator: U.S. Food and Drug Administration
Published: 1981-03-04

Substantially Equivalent

Alba Health Care

FDA 510(k) clearance K803171 for PROCEDURE & RECOVERY PATIENT SUIT, Substantially Equivalent on 1981-03-04. Applicant: Alba Health Care. Device class: 2.

Clearance details

Applicant: Alba Health Care
Product code: Code FYB
Device class: Class 2
Regulation: 21 CFR 878.4040
Advisory panel: General, Plastic Surgery
Date received: 1980-12-15
Decision date: 1981-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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