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)

INTERSCI TEST FOR ALCOHOL IN BODY FLUIDS

K-Number: K792469 · 1980-01-23

ApplicantIntersci Corp.
Decision Date1980-01-23
Product CodeDOJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

INTERSCI TEST FOR ALCOHOL IN BODY FLUIDS is the device name listed in this FDA 510(k) record. The listed applicant is Intersci Corp.. It received FDA 510(k) clearance on 1980-01-23 under 510(k) number K792469. The device is classified under product code DOJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERSCI TEST FOR ALCOHOL IN BODY FLUIDS?

INTERSCI TEST FOR ALCOHOL IN BODY FLUIDS is a medical device that received FDA 510(k) clearance on 1980-01-23. The listed applicant is Intersci Corp.. The 510(k) number is K792469.

When did INTERSCI TEST FOR ALCOHOL IN BODY FLUIDS receive FDA 510(k) clearance?

INTERSCI TEST FOR ALCOHOL IN BODY FLUIDS received FDA 510(k) clearance on 1980-01-23, under 510(k) number K792469.

Who is the listed applicant for INTERSCI TEST FOR ALCOHOL IN BODY FLUIDS?

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

What is the FDA product code for INTERSCI TEST FOR ALCOHOL IN BODY FLUIDS?

The FDA product code for INTERSCI TEST FOR ALCOHOL IN BODY FLUIDS is DOJ.

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

Related Devices (Code: DOJ)

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.

K903223ON-SITE ALCOHOLToxi-Lab, Inc.

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.

↑