Precision Dynamics Corp. - FDA 510(k) Cleared Devices
25
Total
24
Cleared
0
Denied
Precision Dynamics Corp. has 24 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 24 cleared submissions from 1977 to 2002. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Precision Dynamics Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Precision Dynamics Corp.
25 devices
Cleared
Jun 03, 2002
SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE
Obstetrics & Gynecology
90d
Cleared
Mar 22, 2000
SECURELINE DISPOSABLE FETAL MONITORING STRAPS #3860 AND #3565
Obstetrics & Gynecology
90d
Cleared
Jan 24, 2000
SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540
Obstetrics & Gynecology
38d
Cleared
Apr 06, 1999
'ECURLINE UMBILICAL CORD CLAMP #3500
Obstetrics & Gynecology
32d
Cleared
Nov 01, 1988
PRECISION BIOPORT COLLECTION & TRANSPORT SYSTEM
Microbiology
15d
Cleared
Jul 08, 1988
MECHANICAL CHANGE IN IN-VITRO MICRO DEVICE
Microbiology
17d
Cleared
Jan 20, 1988
SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY
General & Plastic Surgery
68d
Cleared
Oct 20, 1987
SECURLINE FRANSEENE NEEDLE
Gastroenterology & Urology
60d
Cleared
Jul 09, 1987
PRECISION CULTURE C.A.T.S. COLLECT/TRANS HSV I/II
Microbiology
15d
Cleared
Aug 27, 1986
AGAR REDUCTION IN FORMULA FOR PDC 110 & 310 MEDIA
Microbiology
9d
Cleared
Apr 22, 1985
FRANZEN NEEDLE GUIDE FOR TRANSRECTAL PROSTATE BIOP
Gastroenterology & Urology
18d
Cleared
Jan 30, 1985
PDC 104 & PDC 304 STYLE CULTURE COLLECTION & TRANS
Microbiology
64d