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

I.V. EXTENDER SET

K Number: K911451 · Decision Jun 6, 1991
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
97
Applicant Total
10
Review Days
64

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Basic Information

Device Name
I.V. EXTENDER SET
K Number
K911451
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Filtertek, Inc.
Date Received
April 3, 1991
Decision Date
June 6, 1991
Product Code
FPB
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
FPB Filter, Infusion Line

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Other Clearances by Filtertek, Inc.

K Number Device Name
K981548 NFC NEEDLEFREE CONNECTOR MODEL 69900
K981547 NFC NEEDLEFREE Y-SITE, MODEL 69970
K914792 PN 62290 0.22 MICRON MICRO INFUS I.V. EXTEN SET
K912848 I.V. FILTER EXTENSION SET
K912394 TRANSDUCER PROTECTOR
K904912 TRANSDUCER PROTECTOR
K901409 TRANSDUCER PROTECTOR
K901996 FILTERTEK PN 60650 DIALYSIS TRANSDUCER PROTECTOR
K895281 TRANSDUCER PROTECTOR