FDA 510(k)

PT PRO-CLOT

K-Number: K874373 · 1988-01-05

Decision Date1988-01-05

Product CodeJBR

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

PT PRO-CLOT is the device name listed in this FDA 510(k) record. The listed applicant is Probe-Tek, Inc.. It received FDA 510(k) clearance on 1988-01-05 under 510(k) number K874373. The device is classified under product code JBR. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PT PRO-CLOT?

PT PRO-CLOT is a medical device that received FDA 510(k) clearance on 1988-01-05. The listed applicant is Probe-Tek, Inc.. The 510(k) number is K874373.

When did PT PRO-CLOT receive FDA 510(k) clearance?

PT PRO-CLOT received FDA 510(k) clearance on 1988-01-05, under 510(k) number K874373.

Who is the listed applicant for PT PRO-CLOT?

The FDA 510(k) record lists Probe-Tek, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PT PRO-CLOT?

The FDA product code for PT PRO-CLOT is JBR.

Other records listing Probe-Tek, Inc. as applicant

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

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