PHILIPS M60 SERIES— 510(k) K920142

Substantially Equivalent

Philips Int'L B.V.

FDA 510(k) clearance K920142 for PHILIPS M60 SERIES, Substantially Equivalent on 1992-01-23. Applicant: Philips Int'L B.V..

Clearance details

Applicant: Philips Int'L B.V.
Product code: Code ESD
Advisory panel: Ear, Nose, Throat
Date received: 1992-01-13
Decision date: 1992-01-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mahwah, NJ, US

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