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FDA 510(k)

ONE INCISION BI-POLAR ELECTRO. FORCEPS

K-Number: K781089 · 1978-07-17

ApplicantKli
Decision Date1978-07-17
Product CodeHIN
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ONE INCISION BI-POLAR ELECTRO. FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Kli. It received FDA 510(k) clearance on 1978-07-17 under 510(k) number K781089. 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 ONE INCISION BI-POLAR ELECTRO. FORCEPS?

ONE INCISION BI-POLAR ELECTRO. FORCEPS is a medical device that received FDA 510(k) clearance on 1978-07-17. The listed applicant is Kli. The 510(k) number is K781089.

When did ONE INCISION BI-POLAR ELECTRO. FORCEPS receive FDA 510(k) clearance?

ONE INCISION BI-POLAR ELECTRO. FORCEPS received FDA 510(k) clearance on 1978-07-17, under 510(k) number K781089.

Who is the listed applicant for ONE INCISION BI-POLAR ELECTRO. FORCEPS?

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 ONE INCISION BI-POLAR ELECTRO. FORCEPS?

The FDA product code for ONE INCISION BI-POLAR ELECTRO. FORCEPS is HIN.

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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 LAPARAOSCOPICK781109FORCEPS, ELECTROSURGICALK780954SCISSORS, HOOK, ELECTROSURGICALK780955SCISSORS, HOOK, ELECTROSURGICAL

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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.

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