The following data is part of a premarket notification filed by Applicare Medical Imaging, B.v. with the FDA for Radworks Medical Imaging Software.
Device ID | K962699 |
510k Number | K962699 |
Device Name: | RADWORKS MEDICAL IMAGING SOFTWARE |
Classification | System, Digital Image Communications, Radiological |
Applicant | APPLICARE MEDICAL IMAGING, B.V. 12300 TWINBROOK PKWY. SUITE 625 Rockville, MD 20852 |
Contact | Robert L Sheridan |
Correspondent | Robert L Sheridan APPLICARE MEDICAL IMAGING, B.V. 12300 TWINBROOK PKWY. SUITE 625 Rockville, MD 20852 |
Product Code | LMD |
CFR Regulation Number | 892.2020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-07-11 |
Decision Date | 1996-08-19 |
Summary: | summary |