The following data is part of a premarket notification filed by Dial-a-rad with the FDA for Dial-a-rad Porta Rad Table.
Device ID | K913425 |
510k Number | K913425 |
Device Name: | DIAL-A-RAD PORTA RAD TABLE |
Classification | Table, Radiographic, Stationary Top |
Applicant | DIAL-A-RAD P.O. BOX 680823 Orlando, FL 32818 |
Contact | Arnold W Morse |
Correspondent | Arnold W Morse DIAL-A-RAD P.O. BOX 680823 Orlando, FL 32818 |
Product Code | IXQ |
CFR Regulation Number | 892.1980 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-08-01 |
Decision Date | 1992-11-24 |