HEADREST, PATIENT COMFORT— 510(k) K882332

Substantially Equivalent

Surgic Aid, Inc.

FDA 510(k) clearance K882332 for HEADREST, PATIENT COMFORT, Substantially Equivalent on 1988-07-19. Applicant: Surgic Aid, Inc.. Device class: 1.

Clearance details

Applicant: Surgic Aid, Inc.
Product code: Code KME
Device class: Class 1
Regulation: 21 CFR 880.6060
Advisory panel: General Hospital
Date received: 1988-06-06
Decision date: 1988-07-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Londonderry, NH, US

Download summary PDF View on FDA.gov ↗

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