FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ACESSORY TO MODIFIED FREEDING JEJUNOSTO

K Number: K813504 · Decision Jan 7, 1982
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
43
Applicant Total
4
Review Days
23

Basic Information

Device Name
ACESSORY TO MODIFIED FREEDING JEJUNOSTO
K Number
K813504
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.4730
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
MIDWEST METABOLIC SUPPORT GROUP
Date Received
December 15, 1981
Decision Date
January 7, 1982
Product Code
KOA
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
KOA Surgical Instruments, G-U, Manual (And Accessories)

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K Number Device Name
K843939 PEDIATRIC SIZE K-TUBE A OR B
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K840019 K-TUBE REPAIR KIT