ADOBE ENTERPRISES SURGICAL/BANDAGE SCISSORS FORCEP— 510(k) K864608

Name: FDA 510(k) clearance K864608
Creator: U.S. Food and Drug Administration
Published: 1986-12-16

Substantially Equivalent

Adobe Ent.

FDA 510(k) clearance K864608 for ADOBE ENTERPRISES SURGICAL/BANDAGE SCISSORS FORCEP, Substantially Equivalent on 1986-12-16. Applicant: Adobe Ent.. Device class: 1.

Clearance details

Applicant: Adobe Ent.
Product code: Code GEN
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1986-11-24
Decision date: 1986-12-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mesa, AZ, US

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