The following data is part of a premarket notification filed by Instromedix, Inc. with the FDA for Lifesigns Receiving Cener 2000 Transtelephonic Receiver.
Device ID | K951096 |
510k Number | K951096 |
Device Name: | LIFESIGNS RECEIVING CENER 2000 TRANSTELEPHONIC RECEIVER |
Classification | Transmitters And Receivers, Electrocardiograph, Telephone |
Applicant | INSTROMEDIX, INC. ONE TECHNOLOGY CENTER 7431 N.E. EVERGREEN PARKWAY Hillsboro, OR 97124 -5898 |
Contact | Herbert J Semler |
Correspondent | Herbert J Semler INSTROMEDIX, INC. ONE TECHNOLOGY CENTER 7431 N.E. EVERGREEN PARKWAY Hillsboro, OR 97124 -5898 |
Product Code | DXH |
CFR Regulation Number | 870.2920 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-03-07 |
Decision Date | 1996-01-16 |