The following data is part of a premarket notification filed by Boehringer Mannheim Corp. with the FDA for Tinaquant Myoglobin Assay.
| Device ID | K972513 |
| 510k Number | K972513 |
| Device Name: | TINAQUANT MYOGLOBIN ASSAY |
| Classification | Myoglobin, Antigen, Antiserum, Control |
| Applicant | BOEHRINGER MANNHEIM CORP. 2400 BISSO LN. Concord, CA 94524 |
| Contact | Yvette Lloyd |
| Correspondent | Yvette Lloyd BOEHRINGER MANNHEIM CORP. 2400 BISSO LN. Concord, CA 94524 |
| Product Code | DDR |
| CFR Regulation Number | 866.5680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-07-07 |
| Decision Date | 1997-07-28 |
| Summary: | summary |