The following data is part of a premarket notification filed by Bayer Corp. with the FDA for 3rd Generation Tsh Assay For The Bayer Immuno 1 System.
| Device ID | K981312 |
| 510k Number | K981312 |
| Device Name: | 3RD GENERATION TSH ASSAY FOR THE BAYER IMMUNO 1 SYSTEM |
| Classification | Radioimmunoassay, Thyroid-stimulating Hormone |
| Applicant | BAYER CORP. 511 BENEDICT AVE. Tarrytown, NY 10591 -5097 |
| Contact | Gabriel J Muraca, Jr. |
| Correspondent | Gabriel J Muraca, Jr. BAYER CORP. 511 BENEDICT AVE. Tarrytown, NY 10591 -5097 |
| Product Code | JLW |
| Subsequent Product Code | JIS |
| Subsequent Product Code | JJX |
| CFR Regulation Number | 862.1690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-04-10 |
| Decision Date | 1998-06-05 |
| Summary: | summary |