ARTHROSCOPE— 510(k) K931792

Substantially Equivalent

Intramed Laboratories, Inc.

FDA 510(k) clearance K931792 for ARTHROSCOPE, Substantially Equivalent on 1994-06-13. Applicant: Intramed Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Intramed Laboratories, Inc.
Product code: Code HRH
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1993-04-12
Decision date: 1994-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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