FDA 510(k)

WHOLE BLOOD PLATELET CONTROL NORMAL,

K-Number: K792606 · 1980-02-13

ApplicantDade, Baxter Travenol Diagnostics, Inc.

Decision Date1980-02-13

Product CodeJPK

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

WHOLE BLOOD PLATELET CONTROL NORMAL, 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 1980-02-13 under 510(k) number K792606. The device is classified under product code JPK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHOLE BLOOD PLATELET CONTROL NORMAL,?

WHOLE BLOOD PLATELET CONTROL NORMAL, is a medical device that received FDA 510(k) clearance on 1980-02-13. The listed applicant is Dade, Baxter Travenol Diagnostics, Inc.. The 510(k) number is K792606.

When did WHOLE BLOOD PLATELET CONTROL NORMAL, receive FDA 510(k) clearance?

WHOLE BLOOD PLATELET CONTROL NORMAL, received FDA 510(k) clearance on 1980-02-13, under 510(k) number K792606.

Who is the listed applicant for WHOLE BLOOD PLATELET CONTROL NORMAL,?

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 WHOLE BLOOD PLATELET CONTROL NORMAL,?

The FDA product code for WHOLE BLOOD PLATELET CONTROL NORMAL, is JPK.

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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.