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FDA 510(k)

BLOOD WARMER (CODE 4R4305)

K-Number: K760012 · 1976-07-16

Decision Date1976-07-16
Product CodeBSB
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

BLOOD WARMER (CODE 4R4305) 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 1976-07-16 under 510(k) number K760012. The device is classified under product code BSB. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD WARMER (CODE 4R4305)?

BLOOD WARMER (CODE 4R4305) is a medical device that received FDA 510(k) clearance on 1976-07-16. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K760012.

When did BLOOD WARMER (CODE 4R4305) receive FDA 510(k) clearance?

BLOOD WARMER (CODE 4R4305) received FDA 510(k) clearance on 1976-07-16, under 510(k) number K760012.

Who is the listed applicant for BLOOD WARMER (CODE 4R4305)?

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 BLOOD WARMER (CODE 4R4305)?

The FDA product code for BLOOD WARMER (CODE 4R4305) is BSB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Travenol Laboratories, S.A. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 206 devices →

Related Devices (Code: BSB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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