Data / Medical devices / United States / Sleep Group Solutions
Sleep Group Solutions: FDA-registered device maker in Hollywood, FL, United States, 3 510(k) clearances
Sleep Group Solutions is registered with the FDA (registration 3007075845) in Hollywood, FL, United States. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated November 9, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007075845
- Address
- 2035 Harding St Ste 200, Hollywood, FL, United States, 33020
- Owner or operator
- Sleep Group Solutions (10024742)
- Roles
- Manufacturer
- First device listed
- February 20, 2008
- Registered through
- 2026
- Brand names listed
- ECCOVISION, SGS Eccovision Pharyngometer, SGS Eccovision Rhinometer
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Rhinoanemometer (Measurement Of Nasal Decongestion) | BXQ | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 9, 2017 | K170071 | SGS ECCOVISIONTM Pharyngometer, SGS ECCOVISIONTM Rhinometer, SGS ECCOVISIONTM Rhino/Pharyngometer | BXQ | Substantially Equivalent | Sleep Group Solutions | accessdata.fda.gov |
| July 26, 2002 | K011329 | ECCOVISION ACOUSTIC DIAGNOSTIC IMAGING ACOUSTIC PHARYNGOMETER | BXQ | Substantially Equivalent | E. Benson Hood Lab, Inc. | accessdata.fda.gov |
| July 8, 1993 | K921452 | ACOUSTIC RHINOMETER | BXQ | Substantially Equivalent | Hood Laboratories | accessdata.fda.gov |
Compare with other makers
Updated November 9, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.