The following data is part of a premarket notification filed by Alexon, Inc. with the FDA for Prospect Giardia Controls.
| Device ID | K922675 |
| 510k Number | K922675 |
| Device Name: | PROSPECT GIARDIA CONTROLS |
| Classification | Giardia Spp. |
| Applicant | ALEXON, INC. 2319 CHARLESTON RD. Mountain View, CA 94043 |
| Contact | Susan Turner |
| Correspondent | Susan Turner ALEXON, INC. 2319 CHARLESTON RD. Mountain View, CA 94043 |
| Product Code | MHI |
| CFR Regulation Number | 866.3220 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-06-04 |
| Decision Date | 1992-09-11 |