H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG— 510(k) K946043
UnknownRudolf Riester GmbH & Co. KG
FDA 510(k) clearance K946043 for H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG, Unknown on 1995-03-08. Applicant: Rudolf Riester GmbH & Co. KG.
Clearance details
- Applicant
- Rudolf Riester GmbH & Co. KG
- Product code
- Code ERA
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- D-72417 Jungingen, DE
Data sourced from openFDA. This site is unofficial and independent of the FDA.