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

SET GRI-FILL 2.0-1 WAY; 2.0-2 WAYS; LUER CONNECTION TUBE

K Number: K033682 · Decision Dec 17, 2003
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
205
Applicant Total
9
Review Days
23

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Basic Information

Device Name
SET GRI-FILL 2.0-1 WAY; 2.0-2 WAYS; LUER CONNECTION TUBE
K Number
K033682
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
November 24, 2003
Decision Date
December 17, 2003
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

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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
K040456 FLEBOSET MULTIPLE
K033916 GRI-BAG, GRI-BAG AP
K031419 GRI-FLEX, MODELS 1000ML, 500ML, 250ML, 100ML