FDA 510(k)

SCISSORS, HOOK, ELECTROSURGICAL

K-Number: K780955 · 1978-06-22

ApplicantKli

Decision Date1978-06-22

Product CodeKNF

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

SCISSORS, HOOK, ELECTROSURGICAL is the device name listed in this FDA 510(k) record. The listed applicant is Kli. It received FDA 510(k) clearance on 1978-06-22 under 510(k) number K780955. The device is classified under product code KNF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCISSORS, HOOK, ELECTROSURGICAL?

SCISSORS, HOOK, ELECTROSURGICAL is a medical device that received FDA 510(k) clearance on 1978-06-22. The listed applicant is Kli. The 510(k) number is K780955.

When did SCISSORS, HOOK, ELECTROSURGICAL receive FDA 510(k) clearance?

SCISSORS, HOOK, ELECTROSURGICAL received FDA 510(k) clearance on 1978-06-22, under 510(k) number K780955.

Who is the listed applicant for SCISSORS, HOOK, ELECTROSURGICAL?

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

What is the FDA product code for SCISSORS, HOOK, ELECTROSURGICAL?

The FDA product code for SCISSORS, HOOK, ELECTROSURGICAL is KNF.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Kli as applicant

K800822CO2 CYSTOSCOPY/URETHROSCOPY CONSOLE K800913GYNECOLOGICAL CYSTO/URETHROSCOPE K781913INSUFFALATOR LAPARAOSCOPIC K781109FORCEPS, ELECTROSURGICAL K781089ONE INCISION BI-POLAR ELECTRO. FORCEPS K780954SCISSORS, HOOK, ELECTROSURGICAL

View all 18 devices →

Related Devices (Code: KNF)

K254303KARL STORZ SUPRALOOPKarl Storz SE & CO. KG K250705Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K240503Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K233848Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-220)Gynesonics, Inc.K222304Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K211535Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, 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.