The following data is part of a premarket notification filed by Windsor Laboratories, Inc. with the FDA for Gentamicin Kit(fpia).
| Device ID | K852013 |
| 510k Number | K852013 |
| Device Name: | GENTAMICIN KIT(FPIA) |
| Classification | Fluorescent Immunoassay Gentamicin |
| 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 | LCQ |
| CFR Regulation Number | 862.3450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-05-09 |
| Decision Date | 1985-06-10 |