The following data is part of a premarket notification filed by Belmont Equipment Corp. with the FDA for Belmont Autopan-pan Oramic, 098e Cephalometric-rad.
Device ID | K852019 |
510k Number | K852019 |
Device Name: | BELMONT AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RAD |
Classification | Unit, X-ray, Intraoral |
Applicant | BELMONT EQUIPMENT CORP. ONE BELMONT DR. Somerset, NJ 08873 |
Contact | John M Gardella |
Correspondent | John M Gardella BELMONT EQUIPMENT CORP. ONE BELMONT DR. Somerset, NJ 08873 |
Product Code | EAP |
CFR Regulation Number | 872.1810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-05-08 |
Decision Date | 1985-06-05 |