ULTRAPAC II SX PLUS (TM)— 510(k) K872657

Substantially Equivalent

Medical Devices, Inc.

FDA 510(k) clearance K872657 for ULTRAPAC II SX PLUS (TM), Substantially Equivalent on 1987-08-04. Applicant: Medical Devices, Inc..

Clearance details

Applicant: Medical Devices, Inc.
Product code: Code GZJ
Advisory panel: Neurology
Date received: 1987-07-07
Decision date: 1987-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

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