MORRISON FRAME, SPECTACLE— 510(k) K940853

Substantially Equivalent

Morrison Center

FDA 510(k) clearance K940853 for MORRISON FRAME, SPECTACLE, Substantially Equivalent on 1994-04-12. Applicant: Morrison Center. Device class: 1.

Clearance details

Applicant
Morrison Center
Product code
Code HQZ
Device class
Class 1
Regulation
21 CFR 886.5842
Advisory panel
Ophthalmic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Palm Florida, FL, US
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