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FDA 510(k)

CAPILLARY FLOW DIALYZERS

K-Number: K840937 · 1984-09-12

ApplicantTravenol Laboratories, S.A.
Decision Date1984-09-12
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CAPILLARY FLOW DIALYZERS 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 1984-09-12 under 510(k) number K840937. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPILLARY FLOW DIALYZERS?

CAPILLARY FLOW DIALYZERS is a medical device that received FDA 510(k) clearance on 1984-09-12. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K840937.

When did CAPILLARY FLOW DIALYZERS receive FDA 510(k) clearance?

CAPILLARY FLOW DIALYZERS received FDA 510(k) clearance on 1984-09-12, under 510(k) number K840937.

Who is the listed applicant for CAPILLARY FLOW DIALYZERS?

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 CAPILLARY FLOW DIALYZERS?

The FDA product code for CAPILLARY FLOW DIALYZERS is KOC.

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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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