NEUROPAC ULTRA I— 510(k) K810593

Substantially Equivalent

Medical Devices, Inc.

FDA 510(k) clearance K810593 for NEUROPAC ULTRA I, Substantially Equivalent on 1981-03-13. Applicant: Medical Devices, Inc..

Clearance details

Applicant: Medical Devices, Inc.
Product code: Code GZJ
Advisory panel: Neurology
Date received: 1981-03-05
Decision date: 1981-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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