FDA 510(k) FDA class 2 Substantially Equivalent - Subject to Tracking Reg. 🇺🇸 United States

FLEXIFLO SIX ENTERAL NUTRITION PUMP

K Number: K943733 · Decision Dec 12, 1994
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
33
Applicant Total
14
Review Days
132

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Basic Information

Device Name
FLEXIFLO SIX ENTERAL NUTRITION PUMP
K Number
K943733
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent - Subject to Tracking Reg.
Applicant
Abbott Mfg., Inc.
Date Received
August 2, 1994
Decision Date
December 12, 1994
Product Code
LZH
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
LZH Pump, Infusion, Enteral

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
K941214 LIFESHIELD EXTENSION SET
Search all 14 clearances from Abbott Mfg., Inc. →