SPINE BOARD— 510(k) K780489

Name: FDA 510(k) clearance K780489
Creator: U.S. Food and Drug Administration
Published: 1978-04-12

Substantially Equivalent

Marullo, Baldwin, Frieden, Gatewood,

FDA 510(k) clearance K780489 for SPINE BOARD, Substantially Equivalent on 1978-04-12. Applicant: Marullo, Baldwin, Frieden, Gatewood,. Device class: 1.

Clearance details

Applicant: Marullo, Baldwin, Frieden, Gatewood,
Product code: Code IQF
Device class: Class 1
Regulation: 21 CFR 890.3490
Advisory panel: Physical Medicine
Date received: 1978-03-27
Decision date: 1978-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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