Jelco Laboratories - FDA 510(k) Cleared Devices
26
Total
26
Cleared
0
Denied
Jelco Laboratories has 26 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 26 cleared submissions from 1976 to 1979. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Jelco Laboratories Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jelco Laboratories
26 devices
Cleared
Oct 02, 1979
JELCO WINGED INTRAVASCULAR CATHETER
General Hospital
7d
Cleared
Sep 12, 1979
JELCO & KVO CATHETER PLACEMENT UNIT
General & Plastic Surgery
50d
Cleared
Jun 27, 1979
CATHETER METAL HUB/RADIOPAQUE
General Hospital
36d
Cleared
Jun 11, 1979
CATHETER METAL HUB/NONRADIOPAQUE
General Hospital
20d
Cleared
Apr 30, 1979
JELCO* DISC FILTER-0.2 MICRON
General Hospital
56d
Cleared
Feb 26, 1979
PROTECTIVSTABILIZER
General & Plastic Surgery
28d
Cleared
Feb 01, 1979
NEEDLE, BLOOD COLLECTING
General & Plastic Surgery
23d
Cleared
Feb 01, 1979
CATHETER TUBING MODIFICATION
Cardiovascular
16d
Cleared
Dec 11, 1978
TRAY, ARTERIAL BLOOD GAS SAMPLING
Anesthesiology
35d
Cleared
Aug 23, 1978
NEEDLES, DESIGN CHANGE, IV CATHETERS
General & Plastic Surgery
85d
Cleared
May 09, 1978
FILTER TUBE
Anesthesiology
39d
Cleared
Dec 02, 1977
J-VAC VACUUM TUBE
Hematology
60d