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

PHARMACIA DELTEC PERIPHERALLY INSERTED VENOUS CATH

K Number: K926544 · Decision Mar 21, 1994
Classifications
1
FEI Numbers
204
Registration Numbers
205
Same Product Code
503
Applicant Total
43
Review Days
445

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Basic Information

Device Name
PHARMACIA DELTEC PERIPHERALLY INSERTED VENOUS CATH
K Number
K926544
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5200
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pharmacia Deltec, Inc.
Date Received
December 31, 1992
Decision Date
March 21, 1994
Product Code
FOZ
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
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

Similar 510(k) Clearances

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Other Clearances by Pharmacia Deltec, Inc.

K Number Device Name
K943310 MODEL 6100 AMBULATORY INFUSION SYSTEM
K942046 PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVE
K942161 LOCKBOX
K942024 PORT-A-CATH LOW PROFILE IMPLANTABLE VENOUS ACCESS SYSTEM
K941445 EXTENSION SET WITH ANTI-SIPHON VALVE
K931073 CATH-FINDER
K932430 DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER
K932433 PHERIPHERALLY INSERTED VENOUS CATHETER-Y SITE
K932198 PHARMACIA DELTEC PERIPHERALLY INSERTED VENOUS CATH
K932464 PERIPHERALLYINSRTED VENOUS CATH. ALTERNATE CATH.
Search all 43 clearances from Pharmacia Deltec, Inc. →