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

STOMACH TUBES

K Number: K800508 · Decision Apr 8, 1980
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
9
Review Days
35

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Basic Information

Device Name
STOMACH TUBES
K Number
K800508
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Medi-Craft , Ltd.
Date Received
March 4, 1980
Decision Date
April 8, 1980
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)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNT), ordered by most recent decision date.

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Other Clearances by Medi-Craft , Ltd.

K Number Device Name
K861949 SUCTION CATHETER KIT
K800510 RECTAL & HARRIS FLUSH TUBES
K800505 URETHRAL CATHETER
K800507 FEEDING TUBES
K800509 CONNECTING TUBES
K800506 OXYGEN CATHETER
K800503 SUCTION CATHETER
K800504 OXYGEN CONNECTING TUBES