PRO-TEC-CASE— 510(k) K950530

Substantially Equivalent

Hyman, Phelps & McNamara, P.C.

FDA 510(k) clearance K950530 for PRO-TEC-CASE, Substantially Equivalent on 1995-04-07. Applicant: Hyman, Phelps & McNamara, P.C..

Clearance details

Applicant: Hyman, Phelps & McNamara, P.C.
Product code: Code LRX
Advisory panel: Ophthalmic
Date received: 1995-02-07
Decision date: 1995-04-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington Dc, DC, US

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