Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LIQUI SOL T4 RIA TEST KIT

K-Number: K770918 · 1977-06-17

ApplicantDamon Corp.
Decision Date1977-06-17
Product CodeCDP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUI SOL T4 RIA TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Damon Corp.. It received FDA 510(k) clearance on 1977-06-17 under 510(k) number K770918. The device is classified under product code CDP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUI SOL T4 RIA TEST KIT?

LIQUI SOL T4 RIA TEST KIT is a medical device that received FDA 510(k) clearance on 1977-06-17. The listed applicant is Damon Corp.. The 510(k) number is K770918.

When did LIQUI SOL T4 RIA TEST KIT receive FDA 510(k) clearance?

LIQUI SOL T4 RIA TEST KIT received FDA 510(k) clearance on 1977-06-17, under 510(k) number K770918.

Who is the listed applicant for LIQUI SOL T4 RIA TEST KIT?

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

What is the FDA product code for LIQUI SOL T4 RIA TEST KIT?

The FDA product code for LIQUI SOL T4 RIA TEST KIT is CDP.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Damon Corp. 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.

K874865DAMON D.E.T.E.C.T IMAGE ENHANCERK831826ADRENOCORTICOTROPIN RADIO-IMMUNOASSAYK820686LIQUISOL PROGESTERONE RADIOIMMUNOK802661LIQUISOL TESTOSTERONE RADIOIMM. TEST KITK790250LIQUISOL CORTISOL RIA TEST KITK782124IEC CENTRA-7 CENTRIFUGE MODEL 2362

View all 11 devices →

Related Devices (Code: CDP)

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.

K001607REPROBEAD T3 ENZYME IMMUNOASSAY REAGENT KIT (CATALOG# 104)Repromedix Corp.K991692CHIRON DIAGNOSTICS ACS: 180 FT3Chiron Diagnostics Corp.K991311TOTAL T3 ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1005Biocheck, Inc.K991252AIA-PACK FT3 ASSAYTosoh Medics, Inc.K981824OPTICOAT T3 EIA KITBiotecx Laboratories, Inc.K983439ABBOTT ARCHITECT FREE T3Abbott Laboratories

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.

↑