LIFETECH CASSETTE— 510(k) K960756

Substantially Equivalent

Lifetech Systems, Inc.

FDA 510(k) clearance K960756 for LIFETECH CASSETTE, Substantially Equivalent on 1997-08-29. Applicant: Lifetech Systems, Inc.. Device class: 2.

Clearance details

Applicant: Lifetech Systems, Inc.
Product code: Code KPJ
Device class: Class 2
Regulation: 21 CFR 878.5650
Advisory panel: General, Plastic Surgery
Date received: 1996-02-23
Decision date: 1997-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fairfax, VA, 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.