Adstation™ 56102A-7
by American Diagnostic Corporation
Adstation™ 56102A-7 is a Class II device made by American Diagnostic Corporation, cleared under FDA 510(k) K950914 on 24 Jul 1995 and listed in FDA GUDID since 21 Sep 2016 (UDI-DI 00634782077433), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00634782077433 | Date21 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK950914 | Date24 Jul 1995 | StatusActive |
Official records
- AccessGUDID record 00634782077433
- FDA 510(k) database K950914
Across registries
- FDA 510(k) K950914 decided 24 Jul 1995 Active
- FDA GUDID UDI-DI 00634782077433 listed 21 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K950914
- Listed FDA GUDID 00634782077433
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Adstation™
- Generic name
- Ophthalmic/otologic diagnostic set
- Model / Ref / Catalog
- 56102A-7
- Primary DI / UDI-DI
- 00634782077433
- 510(k) Number
- FDA product code
- HLJ
- GMDN term
- Ophthalmic/otologic diagnostic set
- Device class
- Class II
- Regulation number
- 886.1570
- GUDID distribution status
- In Commercial Distribution
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