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)

FORCEPS, ELECTROSURGICAL

K-Number: K781109 · 1978-09-14

ApplicantKli
Decision Date1978-09-14
Product CodeHIN
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FORCEPS, ELECTROSURGICAL is the device name listed in this FDA 510(k) record. The listed applicant is Kli. It received FDA 510(k) clearance on 1978-09-14 under 510(k) number K781109. The device is classified under product code HIN. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCEPS, ELECTROSURGICAL?

FORCEPS, ELECTROSURGICAL is a medical device that received FDA 510(k) clearance on 1978-09-14. The listed applicant is Kli. The 510(k) number is K781109.

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

FORCEPS, ELECTROSURGICAL received FDA 510(k) clearance on 1978-09-14, under 510(k) number K781109.

Who is the listed applicant for FORCEPS, 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 FORCEPS, ELECTROSURGICAL?

The FDA product code for FORCEPS, ELECTROSURGICAL is HIN.

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 Kli 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.

K800822CO2 CYSTOSCOPY/URETHROSCOPY CONSOLEK800913GYNECOLOGICAL CYSTO/URETHROSCOPEK781913INSUFFALATOR LAPARAOSCOPICK781089ONE INCISION BI-POLAR ELECTRO. FORCEPSK780954SCISSORS, HOOK, ELECTROSURGICALK780955SCISSORS, HOOK, ELECTROSURGICAL

View all 18 devices →

Related Devices (Code: HIN)

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.

K130305LINA BIPOLAR LOOP; STANDARD SIZE, LARGE SIZE, EXTRA LARGE SIZELina Medical ApsK122983KSEA BIPOLAR ELECTRODEKARL STORZ Endoscopy-America, Inc.K122605PKS BILLGyrus Acmi, Inc.K113080TUBALGATORMectra Labs, Inc.K111751VERSAPOINT II BIPOLAR ELECTROSURGERY GENERATOR, VERSAPOINT II 44MM ANGLED LOOP ELECTRODE, VERSAPOINT II FOOTSWITCH, VERSETHICON, Inc.K111059GYRUS ACMIL BIPOLARLAPROSCOPIC LOOP (PKS BILL)Gyrus Acmi, 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.

↑