The following data is part of a premarket notification filed by Snorex (nz) Ltd. with the FDA for Snorex.
Device ID | K971818 |
510k Number | K971818 |
Device Name: | SNOREX |
Classification | Device, Jaw Repositioning |
Applicant | SNOREX (NZ) LTD. 8210 CARRLEIGH PKWY. Springfield, VA 22152 |
Contact | Vernon Pribble |
Correspondent | Vernon Pribble SNOREX (NZ) LTD. 8210 CARRLEIGH PKWY. Springfield, VA 22152 |
Product Code | LQZ |
CFR Regulation Number | 872.5570 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-05-16 |
Decision Date | 1997-12-18 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SNOREX 98643795 not registered Live/Pending |
MARC J KAYEM MD INC 2024-07-11 |
SNOREX 97092055 not registered Live/Pending |
MARC J KAYEM MD INC 2021-10-26 |
SNOREX 75159035 2160922 Dead/Cancelled |
SELECT NET MARKETING, INC. 1996-08-30 |
SNOREX 74257313 not registered Dead/Abandoned |
SOMTEK, INC. 1992-03-20 |
SNOREX 73597200 not registered Dead/Abandoned |
C.H.S. MARKETING, INC. 1986-05-06 |
SNOREX 73591148 not registered Dead/Abandoned |
UNITED-GUARDIAN, INC. 1986-04-01 |