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

PERCUTANEOUS GASTROINTESTINAL TUBE

K Number: K810499 · Decision Mar 4, 1981
Classifications
1
FEI Numbers
242
Registration Numbers
243
Same Product Code
648
Applicant Total
5
Review Days
8

Basic Information

Device Name
PERCUTANEOUS GASTROINTESTINAL TUBE
K Number
K810499
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
HEALTH DEVELOPMENT CORP.
Date Received
February 24, 1981
Decision Date
March 4, 1981
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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