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

J-VAC VACUUM TUBE

K Number: K771874 · Decision Dec 2, 1977
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
38
Applicant Total
26
Review Days
60

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Basic Information

Device Name
J-VAC VACUUM TUBE
K Number
K771874
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1675
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Jelco Laboratories
Date Received
October 3, 1977
Decision Date
December 2, 1977
Product Code
GIM
Advisory Committee
Clinical Chemistry
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
GIM Tubes, Vacuum Sample, With Anticoagulant

Similar 510(k) Clearances

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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 →