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

GRIPPER PORT-A-CATH NEEDLE WITH STOPCOCK

K Number: K896346 · Decision Jan 18, 1990
Classifications
1
FEI Numbers
437
Registration Numbers
437
Same Product Code
1167
Applicant Total
43
Review Days
76

Basic Information

Device Name
GRIPPER PORT-A-CATH NEEDLE WITH STOPCOCK
K Number
K896346
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
PHARMACIA DELTEC, INC.
Date Received
November 3, 1989
Decision Date
January 18, 1990
Product Code
FPA
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FPA Set, Administration, Intravascular

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K Number Device Name
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K942161 LOCKBOX
K942024 PORT-A-CATH LOW PROFILE IMPLANTABLE VENOUS ACCESS SYSTEM
K941445 EXTENSION SET WITH ANTI-SIPHON VALVE
K931073 CATH-FINDER
K932211 PROCEDURAL TRAY FOR PERIPHERALLY INSERTED VENOUS
K932464 PERIPHERALLYINSRTED VENOUS CATH. ALTERNATE CATH.
K932433 PHERIPHERALLY INSERTED VENOUS CATHETER-Y SITE
K932430 DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER
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