SMARTRECORDER, MODEL 2500— 510(k) K990199

Substantially Equivalent

Respironics, Inc.

FDA 510(k) clearance K990199 for SMARTRECORDER, MODEL 2500, Substantially Equivalent on 1999-04-19. Applicant: Respironics, Inc..

Clearance details

Applicant: Respironics, Inc.
Product code: Code MNR
Advisory panel: Anesthesiology
Date received: 1999-01-21
Decision date: 1999-04-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pittsburgh, PA, US

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