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FDA 510(k)

MEHIGAN-PILLING PHLEBETOME TM

K-Number: K911100 · 1991-06-21

ApplicantPilling Co.
Decision Date1991-06-21
Product CodeMGZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEHIGAN-PILLING PHLEBETOME TM is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1991-06-21 under 510(k) number K911100. The device is classified under product code MGZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEHIGAN-PILLING PHLEBETOME TM?

MEHIGAN-PILLING PHLEBETOME TM is a medical device that received FDA 510(k) clearance on 1991-06-21. The listed applicant is Pilling Co.. The 510(k) number is K911100.

When did MEHIGAN-PILLING PHLEBETOME TM receive FDA 510(k) clearance?

MEHIGAN-PILLING PHLEBETOME TM received FDA 510(k) clearance on 1991-06-21, under 510(k) number K911100.

Who is the listed applicant for MEHIGAN-PILLING PHLEBETOME TM?

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 MEHIGAN-PILLING PHLEBETOME TM?

The FDA product code for MEHIGAN-PILLING PHLEBETOME TM is MGZ.

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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: MGZ)

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.

K260188LimFlow VectorLimFlow, Inc.K250105Boomerang Valvulotome (BMGVT080); Boomerang Push Valvulotome (BMGPVT125)Aveera Medical, Inc.K221902LimFlow VectorLimFlow, Inc.K190267EZE SIT ValvulotomeLemaitre VascularK132047LEMILLS VALVULOTOMELeMaitre Vascular, Inc.K132190EXPANDABLE LEMAITRE VALVULOTOME, OVER-THE-WIRE LEMAITRE VALVULOTOMELeMaitre Vascular, 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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