The following data is part of a premarket notification filed by Coherent Systems, Inc. with the FDA for E-fax Receiver.
| Device ID | K932859 |
| 510k Number | K932859 |
| Device Name: | E-FAX RECEIVER |
| Classification | Transmitters And Receivers, Electrocardiograph, Telephone |
| Applicant | COHERENT SYSTEMS, INC. 1000 BAY AREA BLVD. SUITE 206 Houston, TX 77058 |
| Contact | Tommy Cooper |
| Correspondent | Tommy Cooper COHERENT SYSTEMS, INC. 1000 BAY AREA BLVD. SUITE 206 Houston, TX 77058 |
| Product Code | DXH |
| CFR Regulation Number | 870.2920 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-11 |
| Decision Date | 1994-02-24 |