SCHILLER MODEL SP-100 SPIROVIT(TM)— 510(k) K896120

Name: FDA 510(k) clearance K896120
Creator: U.S. Food and Drug Administration
Published: 1990-01-09

Substantially Equivalent

Schiller America, Inc.

FDA 510(k) clearance K896120 for SCHILLER MODEL SP-100 SPIROVIT(TM), Substantially Equivalent on 1990-01-09. Applicant: Schiller America, Inc.. Device class: 2.

Clearance details

Applicant: Schiller America, Inc.
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 1989-10-24
Decision date: 1990-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tustin, CA, US

Download summary PDF View on FDA.gov ↗

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