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FDA 510(k)

TRANSFER PAK 4R 9006

K-Number: K781811 · 1978-11-08

ApplicantTravenol Laboratories, S.A.
Decision Date1978-11-08
Product CodeKSR
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TRANSFER PAK 4R 9006 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 1978-11-08 under 510(k) number K781811. The device is classified under product code KSR. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSFER PAK 4R 9006?

TRANSFER PAK 4R 9006 is a medical device that received FDA 510(k) clearance on 1978-11-08. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K781811.

When did TRANSFER PAK 4R 9006 receive FDA 510(k) clearance?

TRANSFER PAK 4R 9006 received FDA 510(k) clearance on 1978-11-08, under 510(k) number K781811.

Who is the listed applicant for TRANSFER PAK 4R 9006?

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 TRANSFER PAK 4R 9006?

The FDA product code for TRANSFER PAK 4R 9006 is KSR.

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

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Related Devices (Code: KSR)

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.

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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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