The following data is part of a premarket notification filed by D D S, Inc. with the FDA for Snoremaster.
Device ID | K954128 |
510k Number | K954128 |
Device Name: | SNOREMASTER |
Classification | Device, Anti-snoring |
Applicant | D D S, INC. 2181 ST. ANDREWS RD. Half Moon Bay, CA 94019 |
Contact | Virginia Perry |
Correspondent | Virginia Perry D D S, INC. 2181 ST. ANDREWS RD. Half Moon Bay, CA 94019 |
Product Code | LRK |
CFR Regulation Number | 872.5570 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-09-01 |
Decision Date | 1995-10-02 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00851727004020 | K954128 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SNOREMASTER 74697292 1973090 Dead/Cancelled |
Snoremaster Company, Inc., The 1995-07-05 |
SNOREMASTER 74655546 2263323 Dead/Cancelled |
SNOREMASTER, INC. 1995-04-03 |