FDA 510(k)

T3 UPTAKE DIAG. KIT

K-Number: K771585 · 1977-09-13

Decision Date1977-09-13

Product Code

DecisionSubstantially Equivalent

Device Summary

T3 UPTAKE DIAG. KIT is the device name listed in this FDA 510(k) record. The listed applicant is Antibodies, Inc.. It received FDA 510(k) clearance on 1977-09-13 under 510(k) number K771585. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the T3 UPTAKE DIAG. KIT?

T3 UPTAKE DIAG. KIT is a medical device that received FDA 510(k) clearance on 1977-09-13. The listed applicant is Antibodies, Inc.. The 510(k) number is K771585.

When did T3 UPTAKE DIAG. KIT receive FDA 510(k) clearance?

T3 UPTAKE DIAG. KIT received FDA 510(k) clearance on 1977-09-13, under 510(k) number K771585.

Who is the listed applicant for T3 UPTAKE DIAG. KIT?

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

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Antibodies, Inc. as applicant

K890774GIARDEIA(TM)K843590DETECT-A-STREP K822892CORTISOL RIA KIT K812749ULTRA-DIG K812314CRITHIDNA ANTI-DNA TEST KIT K802877AMIKACIN RIA KIT

View all 16 devices →

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.