The following data is part of a premarket notification filed by Bay X-ray, Inc. with the FDA for Seldix 325 Two Pulse Generator/control.
Device ID | K883154 |
510k Number | K883154 |
Device Name: | SELDIX 325 TWO PULSE GENERATOR/CONTROL |
Classification | Generator, High-voltage, X-ray, Diagnostic |
Applicant | BAY X-RAY, INC. 1630 NORTH MAIN ST., SUITE 101 Walnut Creek, CA 94596 |
Contact | Slobodan Djordjevic |
Correspondent | Slobodan Djordjevic BAY X-RAY, INC. 1630 NORTH MAIN ST., SUITE 101 Walnut Creek, CA 94596 |
Product Code | IZO |
CFR Regulation Number | 892.1700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-07-26 |
Decision Date | 1988-09-06 |