The following data is part of a premarket notification filed by Boehringer Mannheim Corp. with the FDA for Elecsys T-uptake Assay.
| Device ID | K961488 |
| 510k Number | K961488 |
| Device Name: | ELECSYS T-UPTAKE ASSAY |
| Classification | Radioassay, Triiodothyronine Uptake |
| Applicant | BOEHRINGER MANNHEIM CORP. 2400 BISSO LN. P.O. BOX 4117 Concord, CA 94524 -4117 |
| Contact | Mary Koning |
| Correspondent | Mary Koning BOEHRINGER MANNHEIM CORP. 2400 BISSO LN. P.O. BOX 4117 Concord, CA 94524 -4117 |
| Product Code | KHQ |
| CFR Regulation Number | 862.1715 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-04-18 |
| Decision Date | 1996-06-12 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04015630899579 | K961488 | 000 |
| 04015630899548 | K961488 | 000 |