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Biomedical Research & Development Laboratories, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K884693 | UNIVERSAL(TM) ION SELECT ELECTRODE STANDARDS | December 15, 1988 |
| K881655 | SPECTRUM(TM) BLOOD GAS AND ELECTROLYTE CONTROL | May 27, 1988 |
| K834474 | H.P.T. HOME PREG. TEST KIT & A.P.T. | September 28, 1984 |