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FDA 510(k)

TMO OXYGENATOR RESERVOIR PUMP SET

K-Number: K760823 · 1976-11-12

ApplicantTravenol Laboratories, S.A.
Decision Date1976-11-12
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TMO OXYGENATOR RESERVOIR PUMP SET is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1976-11-12 under 510(k) number K760823. The device is classified under product code DTN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TMO OXYGENATOR RESERVOIR PUMP SET?

TMO OXYGENATOR RESERVOIR PUMP SET is a medical device that received FDA 510(k) clearance on 1976-11-12. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K760823.

When did TMO OXYGENATOR RESERVOIR PUMP SET receive FDA 510(k) clearance?

TMO OXYGENATOR RESERVOIR PUMP SET received FDA 510(k) clearance on 1976-11-12, under 510(k) number K760823.

Who is the listed applicant for TMO OXYGENATOR RESERVOIR PUMP SET?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TMO OXYGENATOR RESERVOIR PUMP SET?

The FDA product code for TMO OXYGENATOR RESERVOIR PUMP SET is DTN.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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