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

ENTERAL BAG/SET

K Number: K880051 · Decision Apr 14, 1988
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
35
Review Days
99

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Basic Information

Device Name
ENTERAL BAG/SET
K Number
K880051
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Churchill Corp.
Date Received
January 6, 1988
Decision Date
April 14, 1988
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 Churchill Corp.

K Number Device Name
K880025 CHURCHILL 0.22 MICRON LIQUID FILTER SETS
K880026 CHURCHILL 0.22 MICRON LIQUID COMPACT FILTER SETS
K880027 CHURCHILL 1.2 MICRON LIQUID FILTER SET
K872585 CHURCHILL-CATH
K870395 CHURCHILL PARENTERAL NUTRITION BAG - EVA
K872124 CHURCHILL ALBUMIN IV ADMINISTRATION SET
K872123 CHURCHILL TPN ADMINISTRATION SET
K872043 CHURCHILL INTER-CARDIAC SUCKER
K871084 NITROGLYCERINE PUMP SET
K871085 EXTENSION TUBE PUMP SET
Search all 35 clearances from Churchill Corp. →