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FDA 510(k)

GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP

K-Number: K761169 · 1976-12-09

ApplicantPilling Co.
Decision Date1976-12-09
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K761169. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP?

GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Pilling Co.. The 510(k) number is K761169.

When did GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP receive FDA 510(k) clearance?

GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP received FDA 510(k) clearance on 1976-12-09, under 510(k) number K761169.

Who is the listed applicant for GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP?

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 GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP?

The FDA product code for GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP is DXC.

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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: DXC)

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.

K262086PreludeSYNC™ Radial Compression DeviceMerit Medical Systems, Inc.K260105Fogarty Spring Clips, Handleless Clamps, and Clamp InsertsEdwards LifesciencesK252772Arc Adjustable Radial Cuff Compression DeviceTz Medical, Inc.K254060Life Saving TourniquetTW MedicalK243627Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC)Arc Trauma, LLCK253070Namic Radial Arm Band, 23 cm (DYNJRADBAND); Namic Radial Arm Band, 26 cm (DYNJRADBANDL)Medline Industries, LP

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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