Pioneering Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pioneering Technologies, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Pioneering Technologies, Inc. has 19 FDA 510(k) cleared cardiovascular devices. Based in Martinez, US.
Historical record: 19 cleared submissions from 1988 to 1992.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pioneering Technologies, Inc.
19 devices
Cleared
Sep 22, 1992
ANASTOMART(TM) CORONARY BYPASS GRAFT MARKERS/MODIF
Cardiovascular
168d
Cleared
Feb 14, 1992
PTI ANNULOPLASTY RING(STERILE)
Cardiovascular
452d
Cleared
Dec 31, 1991
PTI INTRA-ART (TM) PICK-UP WICKS
General & Plastic Surgery
417d
Cleared
May 06, 1991
PTI STERNAL CLOSURE WIRE SUTURE
General & Plastic Surgery
117d
Cleared
Mar 18, 1991
PTI ANASTOMARK FLEXIBLE CORONARY BYPASS GRAFT
Cardiovascular
129d
Cleared
Jul 03, 1990
PTI ANASTOMARK(TM) CORONARY BYPASS GRAFT MARKERS
Cardiovascular
84d
Cleared
Jul 03, 1990
MODIFIED STERILIZATION OF INTRA-ART(TM) CORONARY
Cardiovascular
71d
Cleared
Jun 20, 1990
PTI INTRA-ARTR REUSABLE CORONARY ARTERY PROBE
Toxicology
90d
Cleared
May 02, 1990
REUSABLE TENS PARAVERTEBRAL PAD #641 BACK ELECTROD
Neurology
29d
Cleared
Apr 10, 1990
PTI INTRA-ART(TM) ANSARI SAPHENOUS VEIN HOLDER
Cardiovascular
111d
Cleared
Oct 17, 1989
PTI INTRA-ART INTERNAL MAMMARY ARTERY CANNULA KIT
Cardiovascular
84d
Cleared
Oct 12, 1989
PTI INTRA-ART(R) CORONARY ARTERY PROBE (STERILE)
Cardiovascular
202d