LM-300TWIN— 510(k) K913135

Substantially Equivalent

Leisegang Medical, Inc.

FDA 510(k) clearance K913135 for LM-300TWIN, Substantially Equivalent on 1991-09-18. Applicant: Leisegang Medical, Inc.. Device class: 2.

Clearance details

Applicant: Leisegang Medical, Inc.
Product code: Code FSW
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1991-07-16
Decision date: 1991-09-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boca Raton, FL, 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.