FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY

K Number: K854262 · Decision Dec 24, 1985
Classifications
1
FEI Numbers
526
Registration Numbers
526
Same Product Code
18
Applicant Total
24
Review Days
62

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Basic Information

Device Name
MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLY
K Number
K854262
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Meadox Surgimed, Inc.
Date Received
October 23, 1985
Decision Date
December 24, 1985
Product Code
FZX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FZX Guide, Surgical, Instrument

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K930201 ACECUT SUTOMATIC BIOPSY SYSTEM
K911635 MEADOX(R) SURGIMED(R) BIOPSY GUN II
K905181 NO PROFILE OLBERT CATHETER SYSTEM FOR UROLOGY
K904582 QUICKWIRE - HYDROPHILIC COATED GUIDEWIRE
K904983 MEADOX(R) SURGIMED OLBERT CATH SYST FOR UROLOGY
K902461 MEADOX SURGIMED BIOPSY GUN AND NEEDLE
K890926 SURECUT BMB BONE MARROW BIOPSY/ASPIRATION NEEDLE
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