BED BOARD— 510(k) K780230

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K780230 for BED BOARD, Substantially Equivalent on 1978-02-28. Applicant: Biomet, Inc.. Device class: 1.

Clearance details

Applicant: Biomet, Inc.
Product code: Code FPS
Device class: Class 1
Regulation: 21 CFR 880.6070
Advisory panel: General Hospital
Date received: 1978-02-09
Decision date: 1978-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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