Engineering, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Engineering, Inc. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Engineering, Inc. has 4 FDA 510(k) cleared medical devices. Based in Foster City, US.
Historical record: 4 cleared submissions from 1986 to 1988. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Engineering, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Engineering, Inc.
5 devices
Cleared
May 31, 1988
MODIFIED SERVO SYRINGE
Cardiovascular
53d
Cleared
Sep 15, 1986
LS9000 SUCTION BIOPSY NEEDLE
General & Plastic Surgery
56d
Cleared
Jul 18, 1986
LS3000 CANNULA UTERINE SUCTION
Obstetrics & Gynecology
18d
Cleared
Mar 03, 1986
LM2000A SURGICAL SUCTION MONITOR
General Hospital
125d
Cleared
Feb 12, 1986
LS1000 SURGICAL ASPIRATOR II
General & Plastic Surgery
70d