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FDA 510(k)

VARIOUS SIZES & STYLES OF MONOPOLAR FORCEPS

K-Number: K872271 · 1987-06-26

ApplicantNew England Surgical Instrument Corp.
Decision Date1987-06-26
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VARIOUS SIZES & STYLES OF MONOPOLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is New England Surgical Instrument Corp.. It received FDA 510(k) clearance on 1987-06-26 under 510(k) number K872271. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARIOUS SIZES & STYLES OF MONOPOLAR FORCEPS?

VARIOUS SIZES & STYLES OF MONOPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1987-06-26. The listed applicant is New England Surgical Instrument Corp.. The 510(k) number is K872271.

When did VARIOUS SIZES & STYLES OF MONOPOLAR FORCEPS receive FDA 510(k) clearance?

VARIOUS SIZES & STYLES OF MONOPOLAR FORCEPS received FDA 510(k) clearance on 1987-06-26, under 510(k) number K872271.

Who is the listed applicant for VARIOUS SIZES & STYLES OF MONOPOLAR FORCEPS?

The FDA 510(k) record lists New England Surgical Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VARIOUS SIZES & STYLES OF MONOPOLAR FORCEPS?

The FDA product code for VARIOUS SIZES & STYLES OF MONOPOLAR FORCEPS is GEN.

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Other records listing New England Surgical Instrument 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.

K895337ELECTROSURGICAL COAGULATION SUCTION TUBEK895331ELECTROSURGICAL ELECTRODEK883963RANEY AND LEROY-RANEY SCALP CLIPK883396HANDSWITCHING MONOPOLAR PENCILK880863BIPOLAR MICRO COAGULATOR MODELS 25-1000 & 25-1200K880859SURGICAL BURS

View all 18 devices →

Related Devices (Code: GEN)

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.

K031828NATURALASE LP ND:YAG LASERFocus Medical, LLCK953962FORCEPSBiopsys Medical, Inc.K932385SUTURE REMOVING FORCEPSRocket of London, Ltd.K904723FORCEPSMinto Research & Development, Inc.K911159PALPATION PROBENorthgate Technologies, Inc.K900952GS-1200 GRASPING/EXTRACTING FORCEP, 10MMSolos Endoscopy, 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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