1
/
of
0
FDA 510(k), K120371, DR GREENBURGS HYBRID ACRYLIC
FDA 510(k), K120371, DR GREENBURGS HYBRID ACRYLIC
Regular price
$49.00 USD
Regular price
Sale price
$49.00 USD
Unit price
/
per
510(K) Number: K120371
Device Name: DR GREENBURGS HYBRID ACRYLIC
Manufacturer: ALWAYS MORE MARKETING INC
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 02/06/2012
Decision Date: 06/27/2012
Regulation Medical Specialty: Dental
Device Name: DR GREENBURGS HYBRID ACRYLIC
Manufacturer: ALWAYS MORE MARKETING INC
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 02/06/2012
Decision Date: 06/27/2012
Regulation Medical Specialty: Dental
Couldn't load pickup availability
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.
View full details