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

HODGE DECOMPRESSION TUBE

K Number: K834258 · Decision Feb 4, 1984
Classifications
1
FEI Numbers
242
Registration Numbers
243
Same Product Code
648
Applicant Total
32
Review Days
59

Basic Information

Device Name
HODGE DECOMPRESSION TUBE
K Number
K834258
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
INMED CORP.
Date Received
December 7, 1983
Decision Date
February 4, 1984
Product Code
KNT
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
KNT Tubes, Gastrointestinal (And Accessories)

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K850152 PRECONNECTED URETHRAL CATHETER TRAY
K850335 URETEROSCOPY CATHETER
K844801 ULTRA EXTERNAL CATHETER
K842301 DISPOSABLE LATEX BANDAGE
K842866 URETHRAL CATHETERIZATION TRAY
K841040 FOX POST NASAL BALLOON CATHETER
K842865 ESOPHAGEAL STETHOSCOPE
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