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FDA 510(k)

CAROTID ARTERY CLAMP & TOOLS

K-Number: K811821 · 1981-09-24

ApplicantNew England Surgical Instrument Corp.
Decision Date1981-09-24
Product CodeHCE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CAROTID ARTERY CLAMP & TOOLS 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 1981-09-24 under 510(k) number K811821. The device is classified under product code HCE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAROTID ARTERY CLAMP & TOOLS?

CAROTID ARTERY CLAMP & TOOLS is a medical device that received FDA 510(k) clearance on 1981-09-24. The listed applicant is New England Surgical Instrument Corp.. The 510(k) number is K811821.

When did CAROTID ARTERY CLAMP & TOOLS receive FDA 510(k) clearance?

CAROTID ARTERY CLAMP & TOOLS received FDA 510(k) clearance on 1981-09-24, under 510(k) number K811821.

Who is the listed applicant for CAROTID ARTERY CLAMP & TOOLS?

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 CAROTID ARTERY CLAMP & TOOLS?

The FDA product code for CAROTID ARTERY CLAMP & TOOLS is HCE.

Related Clinical Trials

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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 ELECTRODEK895337ELECTROSURGICAL COAGULATION SUCTION TUBEK883963RANEY AND LEROY-RANEY SCALP CLIPK883396HANDSWITCHING MONOPOLAR PENCILK880863BIPOLAR MICRO COAGULATOR MODELS 25-1000 & 25-1200K880859SURGICAL BURS

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Related Devices (Code: HCE)

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.

K870399SELVERSTONE CLAMP SALIBI CLAMPCodman & Shurtleff, 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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