The following data is part of a premarket notification filed by Nihon Kohden America, Inc. with the FDA for Nihon Kohden Zb-831pa Telemetry Transmitter.
Device ID | K946175 |
510k Number | K946175 |
Device Name: | NIHON KOHDEN ZB-831PA TELEMETRY TRANSMITTER |
Classification | Transmitters And Receivers, Physiological Signal, Radiofrequency |
Applicant | NIHON KOHDEN AMERICA, INC. 2601 CAMPUS DR. Irvine, CA 92612 -1601 |
Contact | Penni L Pannell |
Correspondent | Penni L Pannell NIHON KOHDEN AMERICA, INC. 2601 CAMPUS DR. Irvine, CA 92612 -1601 |
Product Code | DRG |
CFR Regulation Number | 870.2910 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-12-19 |
Decision Date | 1995-11-22 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00841983103476 | K946175 | 000 |
00841983103469 | K946175 | 000 |