SCHILLER MODEL SP-200 SPIROVIT(TM)— 510(k) K896121

Substantially Equivalent

Schiller America, Inc.

FDA 510(k) clearance K896121 for SCHILLER MODEL SP-200 SPIROVIT(TM), Substantially Equivalent on 1990-01-09. Applicant: Schiller America, Inc..

Clearance details

Applicant: Schiller America, Inc.
Product code: Code BZG
Advisory panel: Anesthesiology
Date received: 1989-10-24
Decision date: 1990-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tustin, CA, US

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