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FDA 510(k)

ARTERIAL GRAFT SIZERS

K-Number: K761141 · 1977-01-06

ApplicantPilling Co.
Decision Date1977-01-06
Product Code
DecisionSubstantially Equivalent

Device Summary

ARTERIAL GRAFT SIZERS is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1977-01-06 under 510(k) number K761141. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTERIAL GRAFT SIZERS?

ARTERIAL GRAFT SIZERS is a medical device that received FDA 510(k) clearance on 1977-01-06. The listed applicant is Pilling Co.. The 510(k) number is K761141.

When did ARTERIAL GRAFT SIZERS receive FDA 510(k) clearance?

ARTERIAL GRAFT SIZERS received FDA 510(k) clearance on 1977-01-06, under 510(k) number K761141.

Who is the listed applicant for ARTERIAL GRAFT SIZERS?

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

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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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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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