FLOTEC OXYSAVRR (S)— 510(k) K970371

Substantially Equivalent

Flotec, Inc.

FDA 510(k) clearance K970371 for FLOTEC OXYSAVRR (S), Substantially Equivalent on 1997-07-10. Applicant: Flotec, Inc..

Clearance details

Applicant: Flotec, Inc.
Product code: Code NFB
Advisory panel: Anesthesiology
Date received: 1997-01-31
Decision date: 1997-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

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