The following data is part of a premarket notification filed by Varian Medical Systems, Inc. with the FDA for Universal Segmented Cylinder Applicator Set And Universal Stump Applicator Set.
Device ID | K141490 |
510k Number | K141490 |
Device Name: | UNIVERSAL SEGMENTED CYLINDER APPLICATOR SET AND UNIVERSAL STUMP APPLICATOR SET |
Classification | System, Applicator, Radionuclide, Remote-controlled |
Applicant | VARIAN MEDICAL SYSTEMS, INC. 3100 HANSEN WAY Palo Alto, CA 94304 |
Contact | Peter J Coronado |
Correspondent | Peter J Coronado VARIAN MEDICAL SYSTEMS, INC. 3100 HANSEN WAY Palo Alto, CA 94304 |
Product Code | JAQ |
CFR Regulation Number | 892.5700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-06-05 |
Decision Date | 2014-09-26 |
Summary: | summary |