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

KELLY INFLATABLE T DRAIN

K Number: K823428 · Decision Jan 18, 1983
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
473
Applicant Total
3
Review Days
63

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Basic Information

Device Name
KELLY INFLATABLE T DRAIN
K Number
K823428
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Akron Catheter, Inc.
Date Received
November 16, 1982
Decision Date
January 18, 1983
Product Code
FGE
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
FGE Stents, Drains And Dilators For The Biliary Ducts

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Other Clearances by Akron Catheter, Inc.

K Number Device Name
K864736 AKRO-SIL PLUS
K760440 CATHETER, NATURAL LATEX URETHRAL