OSBON PERSONAL LUBRICANT— 510(k) K895406

Name: FDA 510(k) clearance K895406
Creator: U.S. Food and Drug Administration
Published: 1989-12-01

Substantially Equivalent

Osbon Medical Systems, Ltd.

FDA 510(k) clearance K895406 for OSBON PERSONAL LUBRICANT, Substantially Equivalent on 1989-12-01. Applicant: Osbon Medical Systems, Ltd.. Device class: 1.

Clearance details

Applicant: Osbon Medical Systems, Ltd.
Product code: Code KMJ
Device class: Class 1
Regulation: 21 CFR 880.6375
Advisory panel: General Hospital
Date received: 1989-09-06
Decision date: 1989-12-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Augusta, GA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.