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

LIFESHIELD EXTENSION SET

K Number: K941214 · Decision Oct 3, 1994
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
63
Applicant Total
14
Review Days
207

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Basic Information

Device Name
LIFESHIELD EXTENSION SET
K Number
K941214
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Abbott Mfg., Inc.
Date Received
March 10, 1994
Decision Date
October 3, 1994
Product Code
FPK
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
FPK Tubing, Fluid Delivery

Similar 510(k) Clearances

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Other Clearances by Abbott Mfg., Inc.

K Number Device Name
K981457 ALBP
K981232 CA
K981231 CO2
K965230 ABBOTT LIFECARE STANDARD TUBING INFUSION PUMP
K971293 LIFESHIELD PRIMARY I.V. SET WITH BACKCHECK VALVE
K953656 ABBOTT IMX PROLACTIN(MODIFICATION)
K953657 ABBOTT AXSYM PROLACTIN(MODIFICATION)
K944669 FLEXIFLO QUANTUM ENTERAL PUMP
K943691 IMX FOLATE
K943733 FLEXIFLO SIX ENTERAL NUTRITION PUMP
Search all 14 clearances from Abbott Mfg., Inc. →