Swemed Lab International AB is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Swemed Lab International AB - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Swemed Lab International AB has 4 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 4 cleared submissions from 1999 to 2006. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Swemed Lab International AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Swemed Lab International AB
4 devices
Cleared
Jan 30, 2006
CLEAR VISION EMBRYO TRANSFER CATHETER SET, MODEL B100000 - B 100007
Obstetrics & Gynecology
75d
Cleared
Nov 05, 2002
BLASTOMERE BIOPSY PIPETTE, MODELS H-55530 AND H-55540
Obstetrics & Gynecology
89d
Cleared
Aug 18, 1999
SWEMED FOLLICLE ASPIRATION SET, DOUBLE LUMEN, SINGLE LUMEN, AND LUER NEEDLE
Obstetrics & Gynecology
127d
Cleared
Jul 19, 1999
SWEMED INTRACYTOPLASMIC SPERM INJECTION (ICSI) MICRO-INJECTION PIPETTES
Obstetrics & Gynecology
62d