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 IDK954128
510k NumberK954128
Device Name:SNOREMASTER
ClassificationDevice, Anti-snoring
Applicant D D S, INC. 2181 ST. ANDREWS RD. Half Moon Bay,  CA  94019
ContactVirginia Perry
CorrespondentVirginia Perry
D D S, INC. 2181 ST. ANDREWS RD. Half Moon Bay,  CA  94019
Product CodeLRK  
CFR Regulation Number872.5570 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-09-01
Decision Date1995-10-02

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00851727004020 K954128 000

Trademark Results [SNOREMASTER]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SNOREMASTER
SNOREMASTER
74697292 1973090 Dead/Cancelled
Snoremaster Company, Inc., The
1995-07-05
SNOREMASTER
SNOREMASTER
74655546 2263323 Dead/Cancelled
SNOREMASTER, INC.
1995-04-03

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