ANGIOSYS FEMORAL ANGIOGRAPHY DRAPE— 510(k) K843260

Name: FDA 510(k) clearance K843260
Creator: U.S. Food and Drug Administration
Published: 1984-09-21

Substantially Equivalent

Angiosystems, Inc.

FDA 510(k) clearance K843260 for ANGIOSYS FEMORAL ANGIOGRAPHY DRAPE, Substantially Equivalent on 1984-09-21. Applicant: Angiosystems, Inc.. Device class: 2.

Clearance details

Applicant: Angiosystems, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1984-08-20
Decision date: 1984-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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