Cameron-Miller, Inc.
Cameron-Miller, Inc. appears in FDA public data with 0 recalls, 14 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Oct 11, 1994.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K944775 | ELECTROSURGICAL UNIT MODEL 26-0335 | Oct 11, 1994 |
| K931541 | MODEL 26-0375, ELECTROSURGICAL GENERATOR | Jun 1, 1994 |
| K931437 | MODEL 80-1983, ELECTROSURGICAL GENERATOR | May 27, 1994 |
| K935490 | ELECTROSURGICAL DEVICE, MODEL 26-2500 | Apr 1, 1994 |
| K854109 | ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345 | Jan 24, 1986 |
| K853972 | CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATOR | Jan 24, 1986 |
| K833449 | HAND CONTROLLED PENCIL OR SWITCH HAND | Nov 29, 1983 |
| K822092 | CAMERON-MILLER #40-1516 | Sep 21, 1982 |
| K812702 | TECHNICATOR | Nov 5, 1981 |
| K791415 | MODEL 80-1765 ELECTROSURGICAL UNIT | Oct 11, 1979 |
| K781353 | PAPILLOTOME CUTTING SNARE | Oct 10, 1978 |
| K780433 | FIBER OPTIC ADJUSTABLE HEADLIGHT | Jun 13, 1978 |
| K772235 | HAND CONTROL ACCESS.-ELECTROSURG. UNITS | Dec 13, 1977 |
| K771639 | ELECTROSURGICAL GENERATOR | Nov 29, 1977 |