SURGICAL & DENTAL INSTRUMENT— 510(k) K854146

Substantially Equivalent

Baort, Inc.

FDA 510(k) clearance K854146 for SURGICAL & DENTAL INSTRUMENT, Substantially Equivalent on 1985-11-13. Applicant: Baort, Inc.. Device class: 1.

Clearance details

Applicant: Baort, Inc.
Product code: Code GEN
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1985-10-11
Decision date: 1985-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South Orange, NJ, US

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