The following data is part of a premarket notification filed by Ibp Instruments Gmbh with the FDA for Hdm97.
| Device ID | K020908 |
| 510k Number | K020908 |
| Device Name: | HDM97 |
| Classification | Meter, Conductivity, Non-remote |
| Applicant | IBP INSTRUMENTS GMBH SUTELSTR. 7A Hannover, DE 30659 |
| Contact | Werner Pfingstmann |
| Correspondent | Mark Job TUV AMERICA, INC. 1775 OLD HIGHWAY 8 New Brighton, MN 55112 -1891 |
| Product Code | FIZ |
| CFR Regulation Number | 876.5820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2002-03-20 |
| Decision Date | 2002-05-22 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| EIBPHDM97BQ1 | K020908 | 000 |
| EIBPHDM97BH151 | K020908 | 000 |
| EIBPHDM97BH301 | K020908 | 000 |
| EIBPHDM97BH501 | K020908 | 000 |
| EIBPHDM97BH51 | K020908 | 000 |
| EIBPHDM97BL1 | K020908 | 000 |
| EIBPHDM97BM1 | K020908 | 000 |
| EIBPHDM97BN1 | K020908 | 000 |
| EIBPHDM97BO1 | K020908 | 000 |
| EIBPHDM97BP1 | K020908 | 000 |
| EIBPHDM97BH1001 | K020908 | 000 |