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FDA 510(k)

BLOOD FLUID FILTERS

K-Number: K792723 · 1980-01-21

ApplicantDade, Baxter Travenol Diagnostics, Inc.
Decision Date1980-01-21
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BLOOD FLUID FILTERS is the device name listed in this FDA 510(k) record. The listed applicant is Dade, Baxter Travenol Diagnostics, Inc.. It received FDA 510(k) clearance on 1980-01-21 under 510(k) number K792723. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD FLUID FILTERS?

BLOOD FLUID FILTERS is a medical device that received FDA 510(k) clearance on 1980-01-21. The listed applicant is Dade, Baxter Travenol Diagnostics, Inc.. The 510(k) number is K792723.

When did BLOOD FLUID FILTERS receive FDA 510(k) clearance?

BLOOD FLUID FILTERS received FDA 510(k) clearance on 1980-01-21, under 510(k) number K792723.

Who is the listed applicant for BLOOD FLUID FILTERS?

The FDA 510(k) record lists Dade, Baxter Travenol Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD FLUID FILTERS?

The FDA product code for BLOOD FLUID FILTERS is JKA.

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Other records listing Dade, Baxter Travenol Diagnostics, Inc. as applicant

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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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