FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DANTEC DUET

K Number: K960503 · Decision Sep 16, 1996
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
35
Applicant Total
25
Review Days
227

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Basic Information

Device Name
DANTEC DUET
K Number
K960503
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1620
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dantec Medical, Inc.
Date Received
February 2, 1996
Decision Date
September 16, 1996
Product Code
FEN
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FEN Device, Cystometric, Hydraulic

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Other Clearances by Dantec Medical, Inc.

K Number Device Name
K950314 DANTEC MONOPOLAR LUMEN ELECTRODE (13R18 AND 13R19)
K953999 DANTEC DA CAPO
K926363 MULTI-DOP S
K931801 MULTI-DOP X
K930458 MULTI-DOP L
K932059 NEEDLE ELECTRODES AND DISPOSABLE SCALP ELECTRODE
K934580 DANTEC 13R45 BAR ELECTRODE
K931966 DANTEC DISPOSABLE CONCENTRIC NEEDLE
K931923 DANTEC MAGLITE MAGNETIC STIMULATOR (MAGLITE)
K926516 DANTEC MAGNETIC STIMULATOR MAGPRO
Search all 25 clearances from Dantec Medical, Inc. →