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FDA 510(k)

MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY

K-Number: K854262 · 1985-12-24

ApplicantMeadox Surgimed, Inc.
Decision Date1985-12-24
Product CodeFZX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY is the device name listed in this FDA 510(k) record. The listed applicant is Meadox Surgimed, Inc.. It received FDA 510(k) clearance on 1985-12-24 under 510(k) number K854262. The device is classified under product code FZX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY?

MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY is a medical device that received FDA 510(k) clearance on 1985-12-24. The listed applicant is Meadox Surgimed, Inc.. The 510(k) number is K854262.

When did MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY receive FDA 510(k) clearance?

MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY received FDA 510(k) clearance on 1985-12-24, under 510(k) number K854262.

Who is the listed applicant for MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY?

The FDA 510(k) record lists Meadox Surgimed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY?

The FDA product code for MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY is FZX.

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Other records listing Meadox Surgimed, Inc. 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.

K944143MS CLASSIQUE BALLOON CATHETERK945061NOPROFILE OLBERT CATHETER SYSTEMK942382MS AMPLATZ EXTRA STIFF GUIDE WIREK930201ACECUT SUTOMATIC BIOPSY SYSTEMK911635MEADOX(R) SURGIMED(R) BIOPSY GUN IIK905181NO PROFILE OLBERT CATHETER SYSTEM FOR UROLOGY

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Related Devices (Code: FZX)

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.

K914715PARALLELING GUIDESImplant Corp. of AmericaK871413CIVCO STEPPERCIVCO Medical Instruments Co., Inc.K871503BIOPSY NEEDLE GUIDE KIT, STERILEAmedic USAK862564A.C.L. GUIDE KITAspen Laboratories, Inc.K852402NAMIC HOMER MAMMALOK NEEDLE/WIRE LOCALIZERNorth American Instrument Corp.K842698BRITISH SPINAL FUSION SETDowns Surgical , Ltd.

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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