Cameron-Miller, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cameron-Miller, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Cameron-Miller, Inc. has 14 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1977 to 1994.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cameron-Miller, Inc.
14 devices
Cleared
Oct 11, 1994
ELECTROSURGICAL UNIT MODEL 26-0335
General & Plastic Surgery
14d
Cleared
Jun 01, 1994
MODEL 26-0375, ELECTROSURGICAL GENERATOR
Obstetrics & Gynecology
429d
Cleared
May 27, 1994
MODEL 80-1983, ELECTROSURGICAL GENERATOR
Obstetrics & Gynecology
431d
Cleared
Apr 01, 1994
ELECTROSURGICAL DEVICE, MODEL 26-2500
General & Plastic Surgery
137d
Cleared
Jan 24, 1986
CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATOR
General & Plastic Surgery
120d
Cleared
Jan 24, 1986
ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345
General & Plastic Surgery
108d
Cleared
Nov 29, 1983
HAND CONTROLLED PENCIL OR SWITCH HAND
General & Plastic Surgery
55d
Cleared
Sep 21, 1982
CAMERON-MILLER #40-1516
General & Plastic Surgery
67d
Cleared
Nov 05, 1981
TECHNICATOR
General & Plastic Surgery
43d
Cleared
Oct 11, 1979
MODEL 80-1765 ELECTROSURGICAL UNIT
General & Plastic Surgery
72d
Cleared
Oct 10, 1978
PAPILLOTOME CUTTING SNARE
Gastroenterology & Urology
64d
Cleared
Jun 13, 1978
FIBER OPTIC ADJUSTABLE HEADLIGHT
Ophthalmic
88d