The following data is part of a premarket notification filed by Adp Ltd. with the FDA for Adviewer 2000.
Device ID | K952188 |
510k Number | K952188 |
Device Name: | ADVIEWER 2000 |
Classification | Illuminator, Radiographic-film |
Applicant | ADP LTD. 91 SWEDEN ST. P.O. BOX 7764 Haifa, IL 31077 |
Contact | Dan Ben-zeev |
Correspondent | Dan Ben-zeev ADP LTD. 91 SWEDEN ST. P.O. BOX 7764 Haifa, IL 31077 |
Product Code | IXC |
CFR Regulation Number | 892.1890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-05-09 |
Decision Date | 1995-05-30 |