NUCLEOTOME— 510(k) K844131

Name: FDA 510(k) clearance K844131
Creator: U.S. Food and Drug Administration
Published: 1984-11-29

Substantially Equivalent

Medical Instrument Development Laboratories, Inc.

FDA 510(k) clearance K844131 for NUCLEOTOME, Substantially Equivalent on 1984-11-29. Applicant: Medical Instrument Development Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Medical Instrument Development Laboratories, Inc.
Product code: Code HSZ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1984-10-23
Decision date: 1984-11-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Leandro, CA, US

Download summary PDF View on FDA.gov ↗

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