DR. GREENSBURG’S HYBRID


Device Classification Name

device, anti-snoring

510(k) Number K111680
Device Name DR. GREENSBURG’S HYBRID
Applicant
ALWAYS MORE MARKETING INC
4535 w. sahara ave., ste 200
las vegas, 
NV 
89102

Applicant Contact jonathan greenburg
Correspondent
ALWAYS MORE MARKETING INC
4535 w. sahara ave., ste 200
las vegas, 
NV 
89102

Correspodent Contact jonathan greenburg
Regulation Number 872.5570
Classification Product Code
LRK  
Date Received 06/15/2011
Decision Date 12/23/2011
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Dental

510k Review Panel

Dental

summary

summary

Type Abbreviated
Reviewed by Third Party No

Combination Product

No