SPECTRA R PAD— 510(k) K791013

Substantially Equivalent

Parker Laboratories, Inc.

FDA 510(k) clearance K791013 for SPECTRA R PAD, Substantially Equivalent on 1979-09-17. Applicant: Parker Laboratories, Inc..

Clearance details

Applicant: Parker Laboratories, Inc.
Product code: Code GYB
Advisory panel: Neurology
Date received: 1979-06-01
Decision date: 1979-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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