BIOVISION ENDOCULAR PROBE— 510(k) K905115

Name: FDA 510(k) clearance K905115
Creator: U.S. Food and Drug Administration
Published: 1991-02-11

Substantially Equivalent

Douglas James Donaldson Compliance Services

FDA 510(k) clearance K905115 for BIOVISION ENDOCULAR PROBE, Substantially Equivalent on 1991-02-11. Applicant: Douglas James Donaldson Compliance Services. Device class: 2.

Clearance details

Applicant: Douglas James Donaldson Compliance Services
Product code: Code HGF
Device class: Class 2
Regulation: 21 CFR 884.5070
Advisory panel: Obstetrics/Gynecology
Date received: 1990-11-13
Decision date: 1991-02-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oakland, CA, US

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