The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Smith & Nephew Xenon Light Sources And Accessories.
Device ID | K994084 |
510k Number | K994084 |
Device Name: | SMITH & NEPHEW XENON LIGHT SOURCES AND ACCESSORIES |
Classification | Image, Illumination, Fiberoptic, For Endoscope |
Applicant | SMITH & NEPHEW, INC. 160 DASCOMB RD. Andover, MA 01810 |
Contact | Janice Haselton |
Correspondent | Janice Haselton SMITH & NEPHEW, INC. 160 DASCOMB RD. Andover, MA 01810 |
Product Code | FFS |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-12-03 |
Decision Date | 2000-01-20 |
Summary: | summary |