SNOREMASTER
Device, Anti-snoring
D D S, INC.
The following data is part of a premarket notification filed by D D S, Inc. with the FDA for Snoremaster.
Pre-market Notification Details
| 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 |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00851727004020 | K954128 | 000 |
Trademark Results [SNOREMASTER]
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 |
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