Snowden-Pencer is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Snowden-Pencer - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Snowden-Pencer has 10 FDA 510(k) cleared medical devices. Based in Norcross, US.
Historical record: 10 cleared submissions from 1986 to 1996. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Snowden-Pencer Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Snowden-Pencer
10 devices
Cleared
Mar 12, 1996
DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE...
Gastroenterology & Urology
43d
Cleared
May 19, 1994
REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY
General & Plastic Surgery
464d
Cleared
May 16, 1994
REUSABLE LAPAROSCOPIC INSTRUMENTS
General & Plastic Surgery
461d
Cleared
Feb 28, 1994
DIAMOND-SHARP(R) TROCARS
Obstetrics & Gynecology
559d
Cleared
Jan 26, 1993
ENDO I/A PROBE
General & Plastic Surgery
161d
Cleared
Jun 09, 1992
SNOWDEN-PENCER IRRIGATION PUMP
Obstetrics & Gynecology
99d
Cleared
Jun 04, 1992
SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700
Obstetrics & Gynecology
94d
Cleared
Nov 27, 1991
ENDO I/A Y SET
Obstetrics & Gynecology
82d
Cleared
Nov 07, 1991
SNOWDEN-PENCER INSUFFLATOR TUBING SET
Obstetrics & Gynecology
73d
Cleared
Jun 19, 1986
ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORY
General & Plastic Surgery
69d