MODIFIED AOR-SULLIVAN PROTECTIVE OVERGLOVE— 510(k) K902016

Name: FDA 510(k) clearance K902016
Creator: U.S. Food and Drug Administration
Published: 1990-05-16

Substantially Equivalent

Aor-Sullivan

FDA 510(k) clearance K902016 for MODIFIED AOR-SULLIVAN PROTECTIVE OVERGLOVE, Substantially Equivalent on 1990-05-16. Applicant: Aor-Sullivan. Device class: 1.

Clearance details

Applicant: Aor-Sullivan
Product code: Code LYU
Device class: Class 1
Regulation: 21 CFR 878.4040
Advisory panel: General, Plastic Surgery
Date received: 1990-04-30
Decision date: 1990-05-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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