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

#014160-TAB TUBING ROTATOR ADAPTOR

K Number: K870325 · Decision Apr 27, 1987
Classifications
1
FEI Numbers
143
Registration Numbers
144
Same Product Code
136
Applicant Total
10
Review Days
89

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Basic Information

Device Name
#014160-TAB TUBING ROTATOR ADAPTOR
K Number
K870325
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4290
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Clinical Connections, Inc.
Date Received
January 28, 1987
Decision Date
April 27, 1987
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DTL), ordered by most recent decision date.

View all

Other Clearances by Clinical Connections, Inc.

K Number Device Name
K884435 RESUBMITTED 1,3 & 4 WAY STOPCOCKS, VARIOUS PARTS
K871540 SWIVEL CONNECTORS #014452/#014453/#014459-120
K870477 DEVICE CONNECTORS #000299-000 3/8 X 3/8 X 3/8 Y
K870913 INJECTION SITE #014456-120
K870912 T-CONNECTORS 014500/014501/014502/014503-120
K870324 #014460-120 3-WAY & #014461-120 4-WAY STOPCOCK
K870394 HYDROPHOBIC #6194418/HYDRAPHILIC #6104418 FILTERS
K870073 MANIFOLD SWIVEL ROTATOR MODELS 014320 & 014321-TAB
K870326 VARIOUS LUER AND TUBING FITTINGS