LUBRICANT, OTRHO PERSONAL— 510(k) K790087

Name: FDA 510(k) clearance K790087
Creator: U.S. Food and Drug Administration
Published: 1979-02-01

Substantially Equivalent

Ortho Pharmaceutical Corp.

FDA 510(k) clearance K790087 for LUBRICANT, OTRHO PERSONAL, Substantially Equivalent on 1979-02-01. Applicant: Ortho Pharmaceutical Corp.. Device class: 1.

Clearance details

Applicant: Ortho Pharmaceutical Corp.
Product code: Code KMJ
Device class: Class 1
Regulation: 21 CFR 880.6375
Advisory panel: General Hospital
Date received: 1979-01-17
Decision date: 1979-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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K881151 — MICROSCRAPE1988-04-06

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