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)

TOGUARD

K-Number: K790652 · 1979-04-04

ApplicantTogard, Inc.
Decision Date1979-04-04
Product CodeIPG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TOGUARD is the device name listed in this FDA 510(k) record. The listed applicant is Togard, Inc.. It received FDA 510(k) clearance on 1979-04-04 under 510(k) number K790652. The device is classified under product code IPG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOGUARD?

TOGUARD is a medical device that received FDA 510(k) clearance on 1979-04-04. The listed applicant is Togard, Inc.. The 510(k) number is K790652.

When did TOGUARD receive FDA 510(k) clearance?

TOGUARD received FDA 510(k) clearance on 1979-04-04, under 510(k) number K790652.

Who is the listed applicant for TOGUARD?

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

What is the FDA product code for TOGUARD?

The FDA product code for TOGUARD is IPG.

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: IPG)

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.

K024279NESS CHILDREN SYSTEMNess-Neuromuscular Electrical Stimulation SystemsK781363CAST SHOECutler BiomedicalK780617EQUALIZERBallert Orthopedic Corp.K760575ROCKER-SOLE CAST SANDALRichard'S Medical Equip., Inc.K760578BALANCED CAST SOLEParke-Davis Co.

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.

↑