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FDA 510(k)

PILLING BRUSH VALVULOTOME

K-Number: K904507 · 1991-03-01

ApplicantPilling Co.
Decision Date1991-03-01
Product CodeDWQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PILLING BRUSH VALVULOTOME is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1991-03-01 under 510(k) number K904507. The device is classified under product code DWQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PILLING BRUSH VALVULOTOME?

PILLING BRUSH VALVULOTOME is a medical device that received FDA 510(k) clearance on 1991-03-01. The listed applicant is Pilling Co.. The 510(k) number is K904507.

When did PILLING BRUSH VALVULOTOME receive FDA 510(k) clearance?

PILLING BRUSH VALVULOTOME received FDA 510(k) clearance on 1991-03-01, under 510(k) number K904507.

Who is the listed applicant for PILLING BRUSH VALVULOTOME?

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 PILLING BRUSH VALVULOTOME?

The FDA product code for PILLING BRUSH VALVULOTOME is DWQ.

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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

View all 39 devices →

Related Devices (Code: DWQ)

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.

K212894PhasTIPPLeMaitre Vascular, Inc.K041453SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023Smith & Nephew, Inc.K032387TRIVEX SYSTEMSmith & Nephew, Inc.K905528URESIL VALVE CUTTERUresil Corp.K885046INSITUCAT VALVE STRIPPERAesculap Instruments Corp.K872157HALL VEIN STRIPPERSolco Basle, 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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