OXIMETER, IN VIVO CATHETER— 510(k) K760234

Substantially Equivalent

Oximetrix, Inc.

FDA 510(k) clearance K760234 for OXIMETER, IN VIVO CATHETER, Substantially Equivalent on 1976-08-23. Applicant: Oximetrix, Inc..

Clearance details

Applicant: Oximetrix, Inc.
Product code: Code DQE
Advisory panel: Cardiovascular
Date received: 1976-07-15
Decision date: 1976-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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