MULTIPLE, MODEL #17— 510(k) K820823

Substantially Equivalent

Midmark Corp.

FDA 510(k) clearance K820823 for MULTIPLE, MODEL #17, Substantially Equivalent on 1982-04-21. Applicant: Midmark Corp.. Device class: 1.

Clearance details

Applicant: Midmark Corp.
Product code: Code LGX
Device class: Class 1
Regulation: 21 CFR 878.4960
Advisory panel: General, Plastic Surgery
Date received: 1982-03-24
Decision date: 1982-04-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.