The following data is part of a premarket notification filed by Bennett X-ray Corp. with the FDA for Cytoguide Stereotactic Biopsy System Model Mf-cyto.
Device ID | K915201 |
510k Number | K915201 |
Device Name: | CYTOGUIDE STEREOTACTIC BIOPSY SYSTEM MODEL MF-CYTO |
Classification | System, X-ray, Mammographic |
Applicant | BENNETT X-RAY CORP. 54 RAILROAD AVE. Copiague, NY 11726 |
Contact | Schneider |
Correspondent | Schneider BENNETT X-RAY CORP. 54 RAILROAD AVE. Copiague, NY 11726 |
Product Code | IZH |
CFR Regulation Number | 892.1710 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-11-18 |
Decision Date | 1992-07-28 |