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

I-FLOW ELASTOMERIC PUMP (ON-Q, PAINBUSTER, C-BLOC, HOMEPUMP)

K Number: K040337 · Decision May 24, 2004
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
87
Applicant Total
41
Review Days
103

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Basic Information

Device Name
I-FLOW ELASTOMERIC PUMP (ON-Q, PAINBUSTER, C-BLOC, HOMEPUMP)
K Number
K040337
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
I-Flow Corp.
Date Received
February 11, 2004
Decision Date
May 24, 2004
Product Code
MEB
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
MEB Pump, Infusion, Elastomeric

Similar 510(k) Clearances

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

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Other Clearances by I-Flow Corp.

K Number Device Name
K063530 ON-Q, PAINBUSTER, C-BLOC, SELECT-A-FLOW, ONDEMAND, HOMEPUMP, ECLIPSE, C-SERIES, ONE-STEP KVO, EASYPUMP
K063234 ON-Q INTRODUCERS
K051401 ON-Q CATHETER, ON-ANTIMICROBIAL CATHETER, SOAKER CATHETER, I-FLOW CATHETER
K052117 I-FLOW ELASTOMERIC PUMP (ON-Q, PAINBUSTER, C-BLOCK, HOMEPUMP, EASYPUMP)
K043456 MODIFICATION TO SOAKER CATHETER
K023883 HOMEPUMP, ECLIPSE, C-SERIES, PAINBUSTER, C-BLOC, ON-Q, EASYPUMP, KVO
K023827 PARAGON INFUSION SYSTEM WITH BOLUS
K023318 I-FLOW ELASTOMERIC PUMP WITH BOLUS
K022869 SOAKER CATHETER
K020862 I-FLOW ELASTOMERIC PUMP
Search all 41 clearances from I-Flow Corp. →