ELAN-E DISPOSABLE DRAPE— 510(k) K884057

Name: FDA 510(k) clearance K884057
Creator: U.S. Food and Drug Administration
Published: 1988-10-19

Substantially Equivalent

Aesculap Instruments Corp.

FDA 510(k) clearance K884057 for ELAN-E DISPOSABLE DRAPE, Substantially Equivalent on 1988-10-19. Applicant: Aesculap Instruments Corp.. Device class: 2.

Clearance details

Applicant: Aesculap Instruments Corp.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1988-09-26
Decision date: 1988-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlingame, CA, US

Download summary PDF View on FDA.gov ↗

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