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)

WRENCH

K-Number: K791073 · 1979-06-20

ApplicantTruth, Inc.
Decision Date1979-06-20
Product CodeHXC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WRENCH is the device name listed in this FDA 510(k) record. The listed applicant is Truth, Inc.. It received FDA 510(k) clearance on 1979-06-20 under 510(k) number K791073. The device is classified under product code HXC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WRENCH?

WRENCH is a medical device that received FDA 510(k) clearance on 1979-06-20. The listed applicant is Truth, Inc.. The 510(k) number is K791073.

When did WRENCH receive FDA 510(k) clearance?

WRENCH received FDA 510(k) clearance on 1979-06-20, under 510(k) number K791073.

Who is the listed applicant for WRENCH?

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

What is the FDA product code for WRENCH?

The FDA product code for WRENCH is HXC.

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: HXC)

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.

K180092IntellitorqGauthier Biomedical, Inc.K874358COMBINATION WRENCHESMed-Tool, Inc.K874359ADJUSTABLE WRENCHESMed-Tool, Inc.K870053TORQUEDRIVER WRENCHJerome MedicalK813067SPINAL WRENCHTwin City Surgical, 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.

↑