DIGI-INJECTOR— 510(k) K971067

Name: FDA 510(k) clearance K971067
Creator: U.S. Food and Drug Administration
Published: 1997-09-19

Substantially Equivalent

Medical Instrument Development Laboratories, Inc.

FDA 510(k) clearance K971067 for DIGI-INJECTOR, Substantially Equivalent on 1997-09-19. Applicant: Medical Instrument Development Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Medical Instrument Development Laboratories, Inc.
Product code: Code MRH
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1997-03-24
Decision date: 1997-09-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Leandro, CA, US

Download summary PDF View on FDA.gov ↗

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