MICROSCRAPE— 510(k) K881151

Substantially Equivalent

Ortho Pharmaceutical Corp.

FDA 510(k) clearance K881151 for MICROSCRAPE, Substantially Equivalent on 1988-04-06. Applicant: Ortho Pharmaceutical Corp.. Device class: 1.

Clearance details

Applicant: Ortho Pharmaceutical Corp.
Product code: Code LXK
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1988-03-17
Decision date: 1988-04-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raritan, NJ, US

Download summary PDF View on FDA.gov ↗

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