Litton Datamedix
FDA Regulatory Profile
Litton Datamedix appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 21, 1986.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K853599 | LITTON DATAMEDIX BLOOD PRESSURE MONITOR NI | March 21, 1986 |
| K850290 | ULTRASOUND GEL | April 18, 1985 |
| K842497 | SERVOMED OXYMONITO SMK 363 | October 4, 1984 |
| K842312 | SERVOCARD SCP-840 | August 27, 1984 |
| K842235 | SERVOCARD DEFIBRILLATOR SCP-851 | August 27, 1984 |