FDA 510(k) Applications Submitted by KELLER MEDICAL SPECIALTIES PRODUCTS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K982331 | 07/02/1998 | KELLER PULSE OXIMETER, MODEL 850+ | KELLER MEDICAL SPECIALTIES PRODUCTS, INC. |
| K990648 | 03/01/1999 | KELLER VITAL SIGNS MONITOR, KMS 890+ | KELLER MEDICAL SPECIALTIES PRODUCTS, INC. |
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