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FDA 510(k)

DIALYZER, CD-800 COIL

K-Number: K790223 · 1979-03-26

ApplicantTravenol Laboratories, S.A.
Decision Date1979-03-26
Product CodeFHS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIALYZER, CD-800 COIL 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 1979-03-26 under 510(k) number K790223. The device is classified under product code FHS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIALYZER, CD-800 COIL?

DIALYZER, CD-800 COIL is a medical device that received FDA 510(k) clearance on 1979-03-26. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K790223.

When did DIALYZER, CD-800 COIL receive FDA 510(k) clearance?

DIALYZER, CD-800 COIL received FDA 510(k) clearance on 1979-03-26, under 510(k) number K790223.

Who is the listed applicant for DIALYZER, CD-800 COIL?

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 DIALYZER, CD-800 COIL?

The FDA product code for DIALYZER, CD-800 COIL is FHS.

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

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Related Devices (Code: FHS)

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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