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FDA 510(k)

BIPOLAR FORCEPS

K-Number: K912544 · 1991-06-24

ApplicantEverest Medical Corp.
Decision Date1991-06-24
Product CodeMAV
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BIPOLAR 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 1991-06-24 under 510(k) number K912544. The device is classified under product code MAV. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIPOLAR FORCEPS?

BIPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1991-06-24. The listed applicant is Everest Medical Corp.. The 510(k) number is K912544.

When did BIPOLAR FORCEPS receive FDA 510(k) clearance?

BIPOLAR FORCEPS received FDA 510(k) clearance on 1991-06-24, under 510(k) number K912544.

Who is the listed applicant for BIPOLAR 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 BIPOLAR FORCEPS?

The FDA product code for BIPOLAR FORCEPS is MAV.

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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 PROBESK971565BICOAG COAGULATING FORCEPSK955001EVERSHEARS SCISSORS, BILAP PROBES, BICOAG FORCEPS

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Related Devices (Code: MAV)

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.

K260035Digital Indeflator INFLANTEUAB TelemedicinaK220773Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P)Medtronic VascularK162272Fluent inflation deviceVascular Solutions, Inc.K153038Everest 20 Disposable Inflation Device, Everest 20 Survival Kit, Everest 30 Disposable Inflation Device, Everest 30 Survival KitMedtronic, Inc.K153672basixTOUCH40 Inflation SyringeMerit Medical Systems, Inc.K130566BASIXTOUCHMerit Medical Systems, 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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