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FDA 510(k)

ELECTROSURGICAL COAGULATION SUCTION TUBE

K-Number: K895337 · 1989-09-15

ApplicantNew England Surgical Instrument Corp.
Decision Date1989-09-15
Product CodeHAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL COAGULATION SUCTION TUBE 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 1989-09-15 under 510(k) number K895337. The device is classified under product code HAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROSURGICAL COAGULATION SUCTION TUBE?

ELECTROSURGICAL COAGULATION SUCTION TUBE is a medical device that received FDA 510(k) clearance on 1989-09-15. The listed applicant is New England Surgical Instrument Corp.. The 510(k) number is K895337.

When did ELECTROSURGICAL COAGULATION SUCTION TUBE receive FDA 510(k) clearance?

ELECTROSURGICAL COAGULATION SUCTION TUBE received FDA 510(k) clearance on 1989-09-15, under 510(k) number K895337.

Who is the listed applicant for ELECTROSURGICAL COAGULATION SUCTION TUBE?

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 ELECTROSURGICAL COAGULATION SUCTION TUBE?

The FDA product code for ELECTROSURGICAL COAGULATION SUCTION TUBE is HAM.

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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.

K895331ELECTROSURGICAL ELECTRODEK883963RANEY AND LEROY-RANEY SCALP CLIPK883396HANDSWITCHING MONOPOLAR PENCILK880863BIPOLAR MICRO COAGULATOR MODELS 25-1000 & 25-1200K880859SURGICAL BURSK872271VARIOUS SIZES & STYLES OF MONOPOLAR FORCEPS

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Related Devices (Code: HAM)

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.

K153472Quiver Laparoscopic ExtendableItl Corporation Pty, Ltd.K000079NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777MNikomed U.S.A., Inc.K993306NIKOPAD ELECTROSURGICAL GROUNDING PAD (*OR SOLD UNDER COMMERCIAL NAMES), MODEL 4760 (TYPICALLY)Paladin Medical, Inc.K945861BERGEN 710 ESUBergen Mfg.K913300LAPAROSTAT(TM)Cook Ob/GynK920100GSU HANDPIECE ADAPTERBeacon Laboratories, 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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