The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc. with the FDA for Siemens Medical Information Bus (mib Ii) Protocol Converter.
Device ID | K010640 |
510k Number | K010640 |
Device Name: | SIEMENS MEDICAL INFORMATION BUS (MIB II) PROTOCOL CONVERTER |
Classification | Amplifier And Signal Conditioner, Transducer Signal |
Applicant | SIEMENS MEDICAL SOLUTIONS USA, INC. 16 ELECTRONICS AVE. Danvers, MA 01923 |
Contact | Penelope H Greco |
Correspondent | Penelope H Greco SIEMENS MEDICAL SOLUTIONS USA, INC. 16 ELECTRONICS AVE. Danvers, MA 01923 |
Product Code | DRQ |
CFR Regulation Number | 870.2060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-03-05 |
Decision Date | 2001-03-20 |