LIDSPLINT— 510(k) K864810

Substantially Equivalent

Precision Therapeutics, Inc.

FDA 510(k) clearance K864810 for LIDSPLINT, Substantially Equivalent on 1987-01-20. Applicant: Precision Therapeutics, Inc.. Device class: 1.

Clearance details

Applicant: Precision Therapeutics, Inc.
Product code: Code HMP
Device class: Class 1
Regulation: 21 CFR 878.4440
Advisory panel: General, Plastic Surgery
Date received: 1986-12-09
Decision date: 1987-01-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Las Vegas, NV, US

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