FDA 510(k) FDA class 2 Substantially Equivalent 🇪🇸 Spain

FLEBOSET MULTIPLE

K Number: K040456 · Decision Mar 9, 2004
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
205
Applicant Total
9
Review Days
15

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Basic Information

Device Name
FLEBOSET MULTIPLE
K Number
K040456
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Laboratorios Grifols, S.A.
Date Received
February 23, 2004
Decision Date
March 9, 2004
Product Code
LHI
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
Y

Classifications

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

Product Code Device Name
LHI Set, I.V. Fluid Transfer

Similar 510(k) Clearances

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

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Other Clearances by Laboratorios Grifols, S.A.

K Number Device Name
K162216 GRI-FILL PERISTALTIC SET
K102590 FLEBOSET DOUBLE
K093182 SET GRI-FILL 3.0
K082752 QUICKPIN
K050339 SET GRI-FILL 3.0-1 WAY, 2 WAYS, MULTIPLE
K033916 GRI-BAG, GRI-BAG AP
K033682 SET GRI-FILL 2.0-1 WAY; 2.0-2 WAYS; LUER CONNECTION TUBE
K031419 GRI-FLEX, MODELS 1000ML, 500ML, 250ML, 100ML