FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TIMLEINE(TM) VENIPUNCTURE SYSTEM

K Number: K870770 · Decision Apr 23, 1987
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
63
Applicant Total
18
Review Days
56

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Basic Information

Device Name
TIMLEINE(TM) VENIPUNCTURE SYSTEM
K Number
K870770
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5210
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Ipax, Inc.
Date Received
February 26, 1987
Decision Date
April 23, 1987
Product Code
KMK
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
KMK Device, Intravascular Catheter Securement

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K971245 BLINK EXTERNAL EYELID WEIGHT
K915158 SUREBREATH DOME, E-Z BREATHER
K915118 PHACO EMULSIFICATION,IRRIGATION/ASPIRATION TUBE
K914172 KPE 230 AM
K914221 KPE 220 TS, NONSTERILE
K884076 SUREBREATH DOME
K873097 PROCEDUAL CHANGES/ASSEMBLY PROCESS FOR PLUS PAKS
K864726 I/A/KPE TIP
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