The following data is part of a premarket notification filed by Sensus Healthcare with the FDA for Sensus Healthcare Superficial Radiotherapy System Srt-100.
Device ID | K123985 |
510k Number | K123985 |
Device Name: | SENSUS HEALTHCARE SUPERFICIAL RADIOTHERAPY SYSTEM SRT-100 |
Classification | System, Therapeutic, X-ray |
Applicant | SENSUS HEALTHCARE 851 BROKEN SOUND PKWY NW #215 Boca Raton, FL 33487 |
Contact | Kal Fishman |
Correspondent | Kal Fishman SENSUS HEALTHCARE 851 BROKEN SOUND PKWY NW #215 Boca Raton, FL 33487 |
Product Code | JAD |
CFR Regulation Number | 892.5900 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-12-26 |
Decision Date | 2013-05-14 |
Summary: | summary |