Acculmaing
by Radiology Information Systems, Inc.
510(k) K102849
Acculmaing is a medical device (FDA Class II; FDA product code LLZ, System, Image Processing, Radiological) made by Radiology Information Systems, Inc., cleared under FDA 510(k) K102849 on 23 Nov 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 | NumberK102849 | Date23 Nov 2010 | StatusActive |
Official records
- FDA 510(k) database K102849
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LLZ
- Device class
- Class II
- Regulation
- 21 CFR Part 892.2050
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K102849
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 | |||
|---|---|---|---|---|
| Radiology Information Systems, Inc. AccuImaging | AccuImaging | 00860009490628 | — | On the market |
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