The following data is part of a premarket notification filed by Berchtold Holding Gmbh with the FDA for Chromophare E-series.
| Device ID | K080857 |
| 510k Number | K080857 |
| Device Name: | CHROMOPHARE E-SERIES |
| Classification | Light, Surgical, Ceiling Mounted |
| Applicant | BERCHTOLD HOLDING GMBH LUDWIGSTALER STRABE 25 Tuttlingen, DE D-78532 |
| Contact | Silke Goral |
| Correspondent | Jeff D Rongero UNDERWRITERS LABORATORIES, INC. 12 LABORATORY DR. Research Triangle, NC 27709 |
| Product Code | FSY |
| CFR Regulation Number | 878.4580 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2008-03-27 |
| Decision Date | 2008-04-10 |
| Summary: | summary |