The following data is part of a premarket notification filed by American Laboratory Products Co., Ltd. with the FDA for Alpco Milenia Anti-tg Eia.
Device ID | K011415 |
510k Number | K011415 |
Device Name: | ALPCO MILENIA ANTI-TG EIA |
Classification | System, Test, Thyroid Autoantibody |
Applicant | AMERICAN LABORATORY PRODUCTS CO., LTD. P.O. BOX 451 Windham, NH 03087 |
Contact | Richard E Conley |
Correspondent | Richard E Conley AMERICAN LABORATORY PRODUCTS CO., LTD. P.O. BOX 451 Windham, NH 03087 |
Product Code | JZO |
CFR Regulation Number | 866.5870 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-05-08 |
Decision Date | 2001-05-30 |