Accessnet, Accessmed, Accessrad, Medview
by Aspyra, LLC.
510(k) K091631
Accessnet, Accessmed, Accessrad, Medview is a Class II device made by Aspyra, LLC., cleared under FDA 510(k) K091631 on 18 Mar 2010, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK091631 | Date18 Mar 2010 | StatusActive |
Official records
- FDA 510(k) database K091631
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LLZ
- FDA applicant
- Aspyra, Inc.
- Device class
- Class II
- Regulation
- 21 CFR Part 892.2050
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K091631
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| AccessNET 7 | 7 | B433AN0 | — | On the market |
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