FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

GASTROSTOMY REPLACEMENT TUBE, MODEL 253

K Number: K070124 · Decision May 23, 2007
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
19
Review Days
127

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Basic Information

Device Name
GASTROSTOMY REPLACEMENT TUBE, MODEL 253
K Number
K070124
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Degania Silicone , Ltd.
Date Received
January 16, 2007
Decision Date
May 23, 2007
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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Other Clearances by Degania Silicone , Ltd.

K Number Device Name
K254170 Percutaneous Endoscopic Gastrostomy (PEG) Kit
K233591 Stylus
K152246 Aquarius Stoma Measuring Device
K143378 AQUARIUS Gastrostomy Replacement Tube
K141753 AQUARIUS NASAL FEEDING TUBE
K141631 AQUARIUS EXTENSION FEEDING SET
K132686 AQUARIUS LOW PROFILE GASTROSTOMY FEEDING TUBE
K131020 TEMPERATURE SENSOR CATHETER
K122030 LOW PROFILE GASTROSTOMY FEEDING TUBE OR GASTROTOMEY BUTTON
K103371 COUDE/ OR TIEMANN
Search all 19 clearances from Degania Silicone , Ltd. →