The following data is part of a premarket notification filed by Diamond Diagnostics, Inc. with the FDA for Calibrating Material, Calibrating Standards.
| Device ID | K033060 |
| 510k Number | K033060 |
| Device Name: | CALIBRATING MATERIAL, CALIBRATING STANDARDS |
| Classification | Calibrator, Secondary |
| Applicant | DIAMOND DIAGNOSTICS, INC. 331 FISKE ST. Holliston, MA 01746 |
| Contact | Linda M Stundtner |
| Correspondent | Linda M Stundtner DIAMOND DIAGNOSTICS, INC. 331 FISKE ST. Holliston, MA 01746 |
| Product Code | JIT |
| CFR Regulation Number | 862.1150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-09-29 |
| Decision Date | 2004-03-04 |
| Summary: | summary |