NEUROPAC ULTRA II— 510(k) K781829

Substantially Equivalent

Medical Devices, Inc.

FDA 510(k) clearance K781829 for NEUROPAC ULTRA II, Substantially Equivalent on 1978-11-22. Applicant: Medical Devices, Inc..

Clearance details

Applicant: Medical Devices, Inc.
Product code: Code GZJ
Advisory panel: Neurology
Date received: 1978-10-30
Decision date: 1978-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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