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FDA 510(k)

BICOAG COAGULATING FORCEPS

K-Number: K971565 · 1998-03-12

ApplicantEverest Medical Corp.
Decision Date1998-03-12
Product CodeHIN
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BICOAG COAGULATING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Everest Medical Corp.. It received FDA 510(k) clearance on 1998-03-12 under 510(k) number K971565. 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 BICOAG COAGULATING FORCEPS?

BICOAG COAGULATING FORCEPS is a medical device that received FDA 510(k) clearance on 1998-03-12. The listed applicant is Everest Medical Corp.. The 510(k) number is K971565.

When did BICOAG COAGULATING FORCEPS receive FDA 510(k) clearance?

BICOAG COAGULATING FORCEPS received FDA 510(k) clearance on 1998-03-12, under 510(k) number K971565.

Who is the listed applicant for BICOAG COAGULATING FORCEPS?

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

What is the FDA product code for BICOAG COAGULATING FORCEPS?

The FDA product code for BICOAG COAGULATING FORCEPS is HIN.

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Other records listing Everest Medical 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.

K003060PLASMAKINETIC GENERATORK000496EVERSHEARS BIPOLAR SCISSORSK993412BITX PROBESK994336BITX PROBESK955001EVERSHEARS SCISSORS, BILAP PROBES, BICOAG FORCEPSK945975EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS

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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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