Q-PLEX 1— 510(k) K881235

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K881235 for Q-PLEX 1, Substantially Equivalent on 1989-03-31. Applicant: Quinton, Inc..

Clearance details

Applicant: Quinton, Inc.
Product code: Code BZC
Advisory panel: Anesthesiology
Date received: 1988-03-22
Decision date: 1989-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

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