FDA 510(k) Applications Submitted by KAMIYA TECHNOLOGY SERVICES
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K964415 | 10/01/1996 | N-ASSAY TIA RHEUMATOID FACTOR TEST KIT | KAMIYA TECHNOLOGY SERVICES |
| K964418 | 10/01/1996 | N-ASSAY TIA RHEUMATOID FACOTR MULTI-CALIBRATOR SET | KAMIYA TECHNOLOGY SERVICES |
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