FDA 510(k)

T3 STI KIT

K-Number: K780146 · 1978-02-23

Decision Date1978-02-23

Product CodeKHQ

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

T3 STI KIT is the device name listed in this FDA 510(k) record. The listed applicant is Polysciences, Inc.. It received FDA 510(k) clearance on 1978-02-23 under 510(k) number K780146. The device is classified under product code KHQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the T3 STI KIT?

T3 STI KIT is a medical device that received FDA 510(k) clearance on 1978-02-23. The listed applicant is Polysciences, Inc.. The 510(k) number is K780146.

When did T3 STI KIT receive FDA 510(k) clearance?

T3 STI KIT received FDA 510(k) clearance on 1978-02-23, under 510(k) number K780146.

Who is the listed applicant for T3 STI KIT?

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

What is the FDA product code for T3 STI KIT?

The FDA product code for T3 STI KIT is KHQ.

Other records listing Polysciences, 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.

K923349FUNGI FLUOR KIT K871290CENTRICELL(TM)

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Official Source

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