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)

ADRENOCORTICOTROPIC HORMONE TEST

K-Number: K833934 · 1984-04-04

ApplicantClinetics Corp.
Decision Date1984-04-04
Product CodeCKG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ADRENOCORTICOTROPIC HORMONE TEST is the device name listed in this FDA 510(k) record. The listed applicant is Clinetics Corp.. It received FDA 510(k) clearance on 1984-04-04 under 510(k) number K833934. The device is classified under product code CKG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADRENOCORTICOTROPIC HORMONE TEST?

ADRENOCORTICOTROPIC HORMONE TEST is a medical device that received FDA 510(k) clearance on 1984-04-04. The listed applicant is Clinetics Corp.. The 510(k) number is K833934.

When did ADRENOCORTICOTROPIC HORMONE TEST receive FDA 510(k) clearance?

ADRENOCORTICOTROPIC HORMONE TEST received FDA 510(k) clearance on 1984-04-04, under 510(k) number K833934.

Who is the listed applicant for ADRENOCORTICOTROPIC HORMONE TEST?

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

What is the FDA product code for ADRENOCORTICOTROPIC HORMONE TEST?

The FDA product code for ADRENOCORTICOTROPIC HORMONE TEST is CKG.

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 Clinetics 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.

K862180MODIFIED COTROPIN RADIOIMMUNOASSAY KITK844066COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSHK841580TSH RECEPTOR ANTIBODY KIT 125I TSHK830357RADIOIMMUNOASSAY IMMUNOGLOBULINS D.EK823380125-I LH RADIOIMMUNOASSAY KITK823379125-I FSH RADIOIMMUNOASSAY KIT

View all 9 devices →

Related Devices (Code: CKG)

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.

K223867IDS ACTH IIImmunodiagnostic Systems LimitedK111335ST AIA-PACK ACTH, AND ST AIA-PACK ACTH CALIBRATOR SET MODEL 025221 AND 025321Tosoh Bioscience, Inc.K060585ROCHE ELECSYS- ACTH,ACTH CALSET,ACTH CALCHECK,PRECICONTROL ACTHRoche Diagnostics Corp.K050748ACTH IMMUNORADIOMETRIC (IRMA) ASSAY KIT, MODEL 3KG011Scantibodies Laboratory, Inc.K021032ACTH IMMUNORADIOMETRIC (IRMA) DIAGNOSTIC ASSAY KIT, MODEL #3KG100Scantibodies Laboratory, Inc.K002638FUTURE DIAGNOSTICS B.V. STAT-ACTH KITFuture Diagnostics B.V.

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.

↑