Femspec LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Femspec LLC - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Femspec LLC has 4 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Historical record: 4 cleared submissions from 2004 to 2006. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Femspec LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Femspec LLC
4 devices
Cleared
Jul 28, 2006
FEMECC ENDOCERVICAL CURETTE
Obstetrics & Gynecology
170d
Cleared
Feb 02, 2006
FEMSPCE-S DISPOSABLE STERILE VAGINAL SPECULUM, MODEL ST-I
Obstetrics & Gynecology
175d
Cleared
Dec 21, 2005
FEMTEST ENDOMETRIAL SUCTION CURETTE, MODEL FT-1
Obstetrics & Gynecology
217d
Cleared
Dec 23, 2004
FEMSPEC DISPOSABLE VAGINAL SPECULUM
Obstetrics & Gynecology
177d