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FDA 510(k)

BIPOLAR ELECTROSURGICAL SNARE

K-Number: K893553 · 1989-09-08

ApplicantEverest Medical Corp.
Decision Date1989-09-08
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BIPOLAR ELECTROSURGICAL SNARE 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 1989-09-08 under 510(k) number K893553. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIPOLAR ELECTROSURGICAL SNARE?

BIPOLAR ELECTROSURGICAL SNARE is a medical device that received FDA 510(k) clearance on 1989-09-08. The listed applicant is Everest Medical Corp.. The 510(k) number is K893553.

When did BIPOLAR ELECTROSURGICAL SNARE receive FDA 510(k) clearance?

BIPOLAR ELECTROSURGICAL SNARE received FDA 510(k) clearance on 1989-09-08, under 510(k) number K893553.

Who is the listed applicant for BIPOLAR ELECTROSURGICAL SNARE?

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 ELECTROSURGICAL SNARE?

The FDA product code for BIPOLAR ELECTROSURGICAL SNARE is FDI.

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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: FDI)

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.

K251692Advanced Tissue Resection DeviceMicro-Tech (Nanjing) Co., Ltd.K221713Polypectomy SnareHangzhou AGS MedTech Co., Ltd.K220846CORE-SNAREIncore Co., Ltd.K220089Disposable Polyp SnareJiangsu Vedkang Medical Science and Technology Co., Ltd.K220790Disposable Polypectomy Snare, Disposable Polypectomy Hybrid SnareYangzhou Fartley Medical Instrument Technology Co., Ltd.K213222Disposable Polypectomy SnareBeijing Zksk Technology Co., Ltd.

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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