The following data is part of a premarket notification filed by Nextec Corp. with the FDA for Nextec Fiberoptic Illuminat 150 Watt/halo/3500 Kel.
Device ID | K920167 |
510k Number | K920167 |
Device Name: | NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL |
Classification | Illuminator, Fiberoptic, Surgical Field |
Applicant | NEXTEC CORP. 2629 S. HORSESHOE DR. Naples, FL 33942 |
Contact | Jack Kloots |
Correspondent | Jack Kloots NEXTEC CORP. 2629 S. HORSESHOE DR. Naples, FL 33942 |
Product Code | HBI |
CFR Regulation Number | 878.4580 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-01-10 |
Decision Date | 1992-03-23 |