Keller Medical Specialties Products, Inc.
Keller Medical Specialties Products, Inc. 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 August 10, 1999.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K990648 | KELLER VITAL SIGNS MONITOR, KMS 890+ | August 10, 1999 |
| K982331 | KELLER PULSE OXIMETER, MODEL 850+ | September 11, 1998 |
| K914576 | KELLER CARDIAC MONITOR MEDIL KMS870 | December 30, 1991 |
| K910262 | KELLER VITAL SIGNS MONITOR - KMS-890 | April 1, 1991 |
| K903437 | DISPOS ACCESS EXTERNAL CARDIAC PACEMAKER | November 16, 1990 |
| K895987 | KELLER PULSE OXIMETER - KMS 850 | February 22, 1990 |