DREAM CATCHER— 510(k) K972122

Substantially Equivalent

Rest Technologies, Inc.

FDA 510(k) clearance K972122 for DREAM CATCHER, Substantially Equivalent on 1997-08-29. Applicant: Rest Technologies, Inc..

Clearance details

Applicant: Rest Technologies, Inc.
Product code: Code GXY
Advisory panel: Neurology
Date received: 1997-06-05
Decision date: 1997-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Monica, CA, US

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