EYE TRAY— 510(k) K912105

Substantially Equivalent

Medical Device Inspection Co., Inc.

FDA 510(k) clearance K912105 for EYE TRAY, Substantially Equivalent on 1991-08-29. Applicant: Medical Device Inspection Co., Inc..

Clearance details

Applicant: Medical Device Inspection Co., Inc.
Product code: Code LRP
Advisory panel: General, Plastic Surgery
Date received: 1991-05-13
Decision date: 1991-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

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