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

MEADOX SURGIMED A/S THREE PIECE SCREW BIOPSY NEEDL

K Number: K854420 · Decision Nov 22, 1985
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
47
Applicant Total
24
Review Days
18

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Basic Information

Device Name
MEADOX SURGIMED A/S THREE PIECE SCREW BIOPSY NEEDL
K Number
K854420
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
November 4, 1985
Decision Date
November 22, 1985
Product Code
GDM
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
GDM Needle, Aspiration And Injection, Reusable

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Other Clearances by Meadox Surgimed, Inc.

K Number Device Name
K944143 MS CLASSIQUE BALLOON CATHETER
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K942382 MS AMPLATZ EXTRA STIFF GUIDE WIRE
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
Search all 24 clearances from Meadox Surgimed, Inc. →