The following data is part of a premarket notification filed by Always More Marketing Inc with the FDA for Dr Greenburgs Hybrid Vacuum.
| Device ID | K120372 |
| 510k Number | K120372 |
| Device Name: | DR GREENBURGS HYBRID VACUUM |
| Classification | Device, Anti-snoring |
| Applicant | ALWAYS MORE MARKETING INC 4535 W. SAHARA AVE., STE 200 Las Vegas, NV 89102 |
| Contact | Jonathan Greenburg |
| Correspondent | Jonathan Greenburg ALWAYS MORE MARKETING INC 4535 W. SAHARA AVE., STE 200 Las Vegas, NV 89102 |
| Product Code | LRK |
| CFR Regulation Number | 872.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-02-06 |
| Decision Date | 2012-06-27 |
| Summary: | summary |