The following data is part of a premarket notification filed by Xomed-treace, Inc. with the FDA for Xomed-treace Rigid Rod Lens Endoscope.
Device ID | K933105 |
510k Number | K933105 |
Device Name: | XOMED-TREACE RIGID ROD LENS ENDOSCOPE |
Classification | Nasopharyngoscope (flexible Or Rigid) |
Applicant | XOMED-TREACE, INC. 6743 SOUTHPOINT DRIVE NORTH Jacksonville, FL 32216 -0980 |
Contact | Terry Mcmahon |
Correspondent | Terry Mcmahon XOMED-TREACE, INC. 6743 SOUTHPOINT DRIVE NORTH Jacksonville, FL 32216 -0980 |
Product Code | EOB |
CFR Regulation Number | 874.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-06-25 |
Decision Date | 1994-01-05 |