The following data is part of a premarket notification filed by Edan Instruments, Inc. with the FDA for Cadence, Models 2001 And 2002.
Device ID | K040903 |
510k Number | K040903 |
Device Name: | CADENCE, MODELS 2001 AND 2002 |
Classification | System, Monitoring, Perinatal |
Applicant | EDAN INSTRUMENTS, INC. 1 ODELL PLAZA Yonkers, NY 10701 |
Contact | William Stern |
Correspondent | William Stern EDAN INSTRUMENTS, INC. 1 ODELL PLAZA Yonkers, NY 10701 |
Product Code | HGM |
CFR Regulation Number | 884.2740 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-04-07 |
Decision Date | 2004-09-02 |
Summary: | summary |