FDA 510(k) Applications Submitted by EQUAL DIAGNOSTICS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K961179 | 03/26/1996 | SENTINEL LIPASE LIQUID MODEL 17.401B | EQUAL DIAGNOSTICS, INC. |
| K981800 | 05/21/1998 | SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606 | EQUAL DIAGNOSTICS, INC. |
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