The following data is part of a premarket notification filed by Ricarimpex Sas with the FDA for Medicinal Leeches.
Device ID | K040187 |
510k Number | K040187 |
Device Name: | MEDICINAL LEECHES |
Classification | Leeches, Medicinal |
Applicant | RICARIMPEX SAS 245 AVENUE DE SAINT MEDARD 33320 EYSINES France, FR |
Contact | Brigitte Latrille |
Correspondent | Brigitte Latrille RICARIMPEX SAS 245 AVENUE DE SAINT MEDARD 33320 EYSINES France, FR |
Product Code | NRN |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-01-28 |
Decision Date | 2004-06-21 |
Summary: | summary |