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)

HOOK PUNCH FORCEPS FOR ARTHROSCOPY

K-Number: K842819 · 1984-08-14

ApplicantMedtech Industries, Inc.
Decision Date1984-08-14
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HOOK PUNCH FORCEPS FOR ARTHROSCOPY is the device name listed in this FDA 510(k) record. The listed applicant is Medtech Industries, Inc.. It received FDA 510(k) clearance on 1984-08-14 under 510(k) number K842819. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOOK PUNCH FORCEPS FOR ARTHROSCOPY?

HOOK PUNCH FORCEPS FOR ARTHROSCOPY is a medical device that received FDA 510(k) clearance on 1984-08-14. The listed applicant is Medtech Industries, Inc.. The 510(k) number is K842819.

When did HOOK PUNCH FORCEPS FOR ARTHROSCOPY receive FDA 510(k) clearance?

HOOK PUNCH FORCEPS FOR ARTHROSCOPY received FDA 510(k) clearance on 1984-08-14, under 510(k) number K842819.

Who is the listed applicant for HOOK PUNCH FORCEPS FOR ARTHROSCOPY?

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

What is the FDA product code for HOOK PUNCH FORCEPS FOR ARTHROSCOPY?

The FDA product code for HOOK PUNCH FORCEPS FOR ARTHROSCOPY is HTD.

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 Medtech Industries, Inc. 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.

K910451CARD GUARD, MODEL CG-2000AK910450CARD GUARD-3000 ECG TELEPHONE ADAPTERK842820ARTHROSCOPY KNIVES

Related Devices (Code: HTD)

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.

K051281THE NEEDLE CATCHERE.D.Medical , Ltd.K974595CUSHING BAYONET, INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K913964MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSMarlo Surgical TechnologyK911180CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSNorthgate Technologies, 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.

↑