The following data is part of a premarket notification filed by Windsor Laboratories, Inc. with the FDA for Tobramycin Kit(fpia)fluorescence Polarization Immu.
| Device ID | K854392 |
| 510k Number | K854392 |
| Device Name: | TOBRAMYCIN KIT(FPIA)FLUORESCENCE POLARIZATION IMMU |
| Classification | Fluorescence Polarization Immunoassay, Tobramycin |
| Applicant | WINDSOR LABORATORIES, INC. P.O. BOX 475487 Garland, TX 75047 |
| Contact | Guy W Rucker |
| Correspondent | Guy W Rucker WINDSOR LABORATORIES, INC. P.O. BOX 475487 Garland, TX 75047 |
| Product Code | LFW |
| CFR Regulation Number | 862.3900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-10-31 |
| Decision Date | 1985-12-05 |