DISCOGRAPHY KIT— 510(k) K910503

Unknown

B. Braun of America, Inc.

FDA 510(k) clearance K910503 for DISCOGRAPHY KIT, Unknown on 1991-10-07. Applicant: B. Braun of America, Inc.. Device class: 2.

Clearance details

Applicant: B. Braun of America, Inc.
Product code: Code IZG
Device class: Class 2
Regulation: 21 CFR 892.1730
Advisory panel: Radiology
Date received: 1991-02-05
Decision date: 1991-10-07
Decision: Unknown
Clearance type: Traditional
Location: Bethlehem, PA, US

Download summary PDF View on FDA.gov ↗

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K903808 — AMSIS RDS, RADIOGRAPHIC DISCOGRAPHY KIT1991-01-22

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