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FDA 510(k)

KNIFE HANDLE

K-Number: K822203 · 1982-08-20

ApplicantKelleher Corp.
Decision Date1982-08-20
Product CodeKTG
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

KNIFE HANDLE is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-08-20 under 510(k) number K822203. The device is classified under product code KTG. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KNIFE HANDLE?

KNIFE HANDLE is a medical device that received FDA 510(k) clearance on 1982-08-20. The listed applicant is Kelleher Corp.. The 510(k) number is K822203.

When did KNIFE HANDLE receive FDA 510(k) clearance?

KNIFE HANDLE received FDA 510(k) clearance on 1982-08-20, under 510(k) number K822203.

Who is the listed applicant for KNIFE HANDLE?

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

What is the FDA product code for KNIFE HANDLE?

The FDA product code for KNIFE HANDLE is KTG.

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 Kelleher Corp. 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.

K822618EMERGENCY TRACHEOSTOMY INSTRUMENT SETK822268NAGASHIMA NS-III ELECTRONYSTAGMOGRAPHK823083ELECTROSURGICAL UNITK822252ENT TREATMENT UNITSK823111NYSTYMOGRAPH ACCESSK822272HEAD MIRRORS W/HEAD LAMPS & HEAD BANDS

View all 94 devices →

Related Devices (Code: KTG)

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.

K822205KNIVES, ENTKelleher Corp.K822280ENT KNIFE HANDLESKelleher Corp.K822279LANCETS FOR EAR SURGERYKelleher Corp.K822187TONSIL DISSECTORSKelleher Corp.

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.

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