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FDA 510(k)

CAROTID ARTERY ARTERIOTOMY CLOSURE CLAMP

K-Number: K760645 · 1976-09-21

ApplicantPilling Co.
Decision Date1976-09-21
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CAROTID ARTERY ARTERIOTOMY CLOSURE CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1976-09-21 under 510(k) number K760645. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAROTID ARTERY ARTERIOTOMY CLOSURE CLAMP?

CAROTID ARTERY ARTERIOTOMY CLOSURE CLAMP is a medical device that received FDA 510(k) clearance on 1976-09-21. The listed applicant is Pilling Co.. The 510(k) number is K760645.

When did CAROTID ARTERY ARTERIOTOMY CLOSURE CLAMP receive FDA 510(k) clearance?

CAROTID ARTERY ARTERIOTOMY CLOSURE CLAMP received FDA 510(k) clearance on 1976-09-21, under 510(k) number K760645.

Who is the listed applicant for CAROTID ARTERY ARTERIOTOMY CLOSURE CLAMP?

The FDA 510(k) record lists Pilling Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAROTID ARTERY ARTERIOTOMY CLOSURE CLAMP?

The FDA product code for CAROTID ARTERY ARTERIOTOMY CLOSURE CLAMP is DWS.

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Other records listing Pilling Co. 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.

K934427PILLING LAPAROSCOPIC INSTRUMENTATIONK925370TRIANGULAR JAW MICROLARYNGEAL FORCEPSK925198KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTRK922971NO-SCALPEL VASCETOMY INSTRUMENTSK914015CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMPK911099MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE

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Related Devices (Code: DWS)

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.

K022238MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626Medtronic VascularK964445OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006)Dlp, Inc.K962771BURKE CONGENITAL THORACOSCOPY INSTRUMENTSPilling Weck, Inc.K955689RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAYContour Fabricators of Florida, Inc.K960139G.E. STERILE ANGIOGRAPHIC TRAYGE Medical SystemsK960144G.E. STERILE CT BIOPSY TRAYGE Medical Systems

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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