The following data is part of a premarket notification filed by Kbl Ag with the FDA for Kbl Sunlamp Products (= Device Bundling Name).
| Device ID | K151962 |
| 510k Number | K151962 |
| Device Name: | KBL Sunlamp Products (= Device Bundling Name) |
| Classification | Booth, Sun Tan |
| Applicant | KBL AG RINGSTRASSE 24-26 Dernbach, DE 56307 |
| Contact | Norbert Becker |
| Correspondent | Norbert Becker KBL AG RINGSTRASSE 24-26 Dernbach, DE 56307 |
| Product Code | LEJ |
| CFR Regulation Number | 878.4635 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-07-16 |
| Decision Date | 2016-09-15 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04260489020111 | K151962 | 000 |
| 04260489020401 | K151962 | 000 |
| 04260489020357 | K151962 | 000 |
| 04260489020364 | K151962 | 000 |
| 04260489020388 | K151962 | 000 |
| 04260489020227 | K151962 | 000 |
| 04260489020173 | K151962 | 000 |
| 04260489020241 | K151962 | 000 |
| 04260489020258 | K151962 | 000 |
| 04260489020265 | K151962 | 000 |
| 04260489020272 | K151962 | 000 |
| 04260489020234 | K151962 | 000 |
| 04260489020203 | K151962 | 000 |
| 04260489020081 | K151962 | 000 |
| 04260489020098 | K151962 | 000 |
| 04260489020104 | K151962 | 000 |
| 04260489020418 | K151962 | 000 |