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

DISPOSABLE STOPCOCK

K Number: K861783 · Decision Jul 17, 1986
Classifications
1
FEI Numbers
149
Registration Numbers
150
Same Product Code
137
Applicant Total
38
Review Days
70

Basic Information

Device Name
DISPOSABLE STOPCOCK
K Number
K861783
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4290
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
UTAH MEDICAL PRODUCTS, INC.
Date Received
May 8, 1986
Decision Date
July 17, 1986
Product Code
DTL
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DTL Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

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