SPECTRUM DESIGNS SPECTRAGEL— 510(k) K970702

Substantially Equivalent

Spectrum Designs, Inc.

FDA 510(k) clearance K970702 for SPECTRUM DESIGNS SPECTRAGEL, Substantially Equivalent on 1997-05-12. Applicant: Spectrum Designs, Inc..

Clearance details

Applicant: Spectrum Designs, Inc.
Product code: Code MDA
Advisory panel: General, Plastic Surgery
Date received: 1997-02-26
Decision date: 1997-05-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Goleta, CA, US

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