FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

DoubleChek DC-1001

K Number: K212316 · Decision Sep 30, 2022
Classifications
1
FEI Numbers
242
Registration Numbers
243
Same Product Code
648
Applicant Total
1
Review Days
431

Basic Information

Device Name
DoubleChek DC-1001
K Number
K212316
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nasogastric Feeding Solutions, Ltd.
Date Received
July 26, 2021
Decision Date
September 30, 2022
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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