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

I.V. LOK TM

K Number: K770119 · Decision Mar 14, 1977
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
63
Applicant Total
26
Review Days
52

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Basic Information

Device Name
I.V. LOK TM
K Number
K770119
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5210
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Jelco Laboratories
Date Received
January 21, 1977
Decision Date
March 14, 1977
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

Similar 510(k) Clearances

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

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Other Clearances by Jelco Laboratories

K Number Device Name
K791918 JELCO WINGED INTRAVASCULAR CATHETER
K791372 JELCO & KVO CATHETER PLACEMENT UNIT
K790967 CATHETER METAL HUB/RADIOPAQUE
K790968 CATHETER METAL HUB/NONRADIOPAQUE
K790471 JELCO* DISC FILTER-0.2 MICRON
K790186 PROTECTIVSTABILIZER
K790079 NEEDLE, BLOOD COLLECTING
K790107 CATHETER TUBING MODIFICATION
K781857 TRAY, ARTERIAL BLOOD GAS SAMPLING
K780896 NEEDLES, DESIGN CHANGE, IV CATHETERS
Search all 26 clearances from Jelco Laboratories →