The following data is part of a premarket notification filed by Bennett X-ray Corp. with the FDA for Vertical Integrated Perfect View (vip) Radiographic System.
Device ID | K952672 |
510k Number | K952672 |
Device Name: | VERTICAL INTEGRATED PERFECT VIEW (VIP) RADIOGRAPHIC SYSTEM |
Classification | System, X-ray, Stationary |
Applicant | BENNETT X-RAY CORP. 445 OAK ST. Copiague, NY 11726 |
Contact | Robert P Coe |
Correspondent | Robert P Coe BENNETT X-RAY CORP. 445 OAK ST. Copiague, NY 11726 |
Product Code | KPR |
CFR Regulation Number | 892.1680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-06-12 |
Decision Date | 1995-07-13 |