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FDA 510(k)

SURGIMED BREAST LOCALIZATION NEEDLE WIRE SET

K-Number: K936226 · 1994-03-07

ApplicantMeadox Medicals, Div. Boston Scientific Corp.
Decision Date1994-03-07
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGIMED BREAST LOCALIZATION NEEDLE WIRE SET is the device name listed in this FDA 510(k) record. The listed applicant is Meadox Medicals, Div. Boston Scientific Corp.. It received FDA 510(k) clearance on 1994-03-07 under 510(k) number K936226. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGIMED BREAST LOCALIZATION NEEDLE WIRE SET?

SURGIMED BREAST LOCALIZATION NEEDLE WIRE SET is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Meadox Medicals, Div. Boston Scientific Corp.. The 510(k) number is K936226.

When did SURGIMED BREAST LOCALIZATION NEEDLE WIRE SET receive FDA 510(k) clearance?

SURGIMED BREAST LOCALIZATION NEEDLE WIRE SET received FDA 510(k) clearance on 1994-03-07, under 510(k) number K936226.

Who is the listed applicant for SURGIMED BREAST LOCALIZATION NEEDLE WIRE SET?

The FDA 510(k) record lists Meadox Medicals, Div. Boston Scientific Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGIMED BREAST LOCALIZATION NEEDLE WIRE SET?

The FDA product code for SURGIMED BREAST LOCALIZATION NEEDLE WIRE SET is KDC.

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Other records listing Meadox Medicals, Div. Boston Scientific Corp. as applicant

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Related Devices (Code: KDC)

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.

K943229DISPOSABLE SURGICAL SCISSORS AND FORCEPSY.M.K. International Co., Ltd.K920153THERMUFF BAGTechstylesK920263MANUAL SURGICAL INSTRUMENTSPhoenix Instruments Div.K915064DISPOSABLE CAUTERY ABRASIVE PADAmerican Medical Mfg., Inc.K914960INSTRUMENT ORGANIZERO.R. Concepts, Inc.K912834SHUR-GRIPInman Medical Corp.

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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