The following data is part of a premarket notification filed by Varian Medical Systems, Inc. with the FDA for Surface Applicator Set.
| Device ID | K162018 |
| 510k Number | K162018 |
| Device Name: | Surface Applicator Set |
| Classification | System, Applicator, Radionuclide, Remote-controlled |
| Applicant | Varian Medical Systems, Inc. 911 Hansen Way Palo Alto, CA 94304 |
| Contact | Peter J. Coronado |
| Correspondent | Peter J. Coronado Varian Medical Systems, Inc. 911 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 | 2016-07-14 |
| Decision Date | 2017-02-28 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00816389022805 | K162018 | 000 |
| 00816389022799 | K162018 | 000 |
| 00816389022744 | K162018 | 000 |
| 00816389022737 | K162018 | 000 |
| 00816389022720 | K162018 | 000 |
| 00816389022607 | K162018 | 000 |
| 00810563021950 | K162018 | 000 |