The following data is part of a premarket notification filed by Boehringer Mannheim Corp. with the FDA for Modification Of Preciset Serum Proteins Calibrator.
| Device ID | K984425 |
| 510k Number | K984425 |
| Device Name: | MODIFICATION OF PRECISET SERUM PROTEINS CALIBRATOR |
| Classification | Calibrator, Multi-analyte Mixture |
| Applicant | BOEHRINGER MANNHEIM CORP. 9115 HAGUE RD. Indianapolis, IN 46250 -0457 |
| Contact | Priscilla A Hamill |
| Correspondent | Priscilla A Hamill BOEHRINGER MANNHEIM CORP. 9115 HAGUE RD. Indianapolis, IN 46250 -0457 |
| Product Code | JIX |
| CFR Regulation Number | 862.1150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-12-11 |
| Decision Date | 1999-01-20 |
| Summary: | summary |