Mennen Greatbatch Electonics
Mennen Greatbatch Electonics appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 22, 1977.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K772000 | ECG TELEMETRY SYSTEM | November 22, 1977 |
| K770832 | PORTASCOPE II | June 3, 1977 |
| K770279 | MONITOR, PORTABLE, PART #431-010 | February 24, 1977 |
| K770247 | D.C. AMPLIFIER MODULE | February 14, 1977 |
| K770246 | ISOLATED EEG AMPLIFIER MODULE | February 14, 1977 |
| K770245 | ABDOMINAL FETAL ECG MODULE | February 14, 1977 |