PROGEL(TM), MODELS 8630 AND 8635— 510(k) K882887

Substantially Equivalent

Medical Devices, Inc.

FDA 510(k) clearance K882887 for PROGEL(TM), MODELS 8630 AND 8635, Substantially Equivalent on 1988-09-29. Applicant: Medical Devices, Inc..

Clearance details

Applicant: Medical Devices, Inc.
Product code: Code GXY
Advisory panel: Neurology
Date received: 1988-07-11
Decision date: 1988-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

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