Company ยท US
Keller Medical Specialties Products, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 1999. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 10, 1999 | K990648 | KELLER VITAL SIGNS MONITOR, KMS 890+ Keller Medical Specialties Products, Inc. | DXN |
| Sep 11, 1998 | K982331 | KELLER PULSE OXIMETER, MODEL 850+ Keller Medical Specialties Products, Inc. | DQA |
| Dec 30, 1991 | K914576 | KELLER CARDIAC MONITOR MEDIL KMS870 Keller Medical Specialties Products, Inc. | DRT |
| Apr 1, 1991 | K910262 | KELLER VITAL SIGNS MONITOR - KMS-890 Keller Medical Specialties Products, Inc. | DSJ |
| Nov 16, 1990 | K903437 | DISPOS ACCESS EXTERNAL CARDIAC PACEMAKER Keller Medical Specialties Products, Inc. | DRO |
| Feb 22, 1990 | K895987 | KELLER PULSE OXIMETER - KMS 850 Keller Medical Specialties Products, Inc. | DQA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||