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)

ATROXIN

K-Number: K780355 · 1978-04-18

ApplicantSigma Chemical Co.
Decision Date1978-04-18
Product CodeJCO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

ATROXIN is the device name listed in this FDA 510(k) record. The listed applicant is Sigma Chemical Co.. It received FDA 510(k) clearance on 1978-04-18 under 510(k) number K780355. The device is classified under product code JCO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATROXIN?

ATROXIN is a medical device that received FDA 510(k) clearance on 1978-04-18. The listed applicant is Sigma Chemical Co.. The 510(k) number is K780355.

When did ATROXIN receive FDA 510(k) clearance?

ATROXIN received FDA 510(k) clearance on 1978-04-18, under 510(k) number K780355.

Who is the listed applicant for ATROXIN?

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

What is the FDA product code for ATROXIN?

The FDA product code for ATROXIN is JCO.

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 Sigma Chemical Co. 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.

K933694SIGMA GLUCOSE REAGENTK933678SIGMA CALCIUM REAGENTK933696SIGMA ELECTROLYTE REFERENCE REAGENTK933679SIGMA BUN REAGENTK933691SIGMA CO2 ALKALINE BUFFER REAGENTK933703SIGMA WASH CONCENTRATE SOLUTION

View all 231 devices →

Related Devices (Code: JCO)

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.

K955115VENOM TIEM REAGENTMedical Diagnostic Technologies, Inc.K932787BATROXOBIN REAGENTBehring Diagnostics, Inc.K896033FDP COLLECTION TUBESMedical Diagnostic Technologies, Inc.K852519DUPONT ACA FIBRIN DEGRADATION PROD CLOTTING TUBEE.I. Dupont DE Nemours & Co., Inc.K843207REPTILASE -PCBio/Data Corp.K840210REPTILASE-R HA35Wellcome Diagnostics

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.

↑