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PalmScan DA2000
Micro Medical Devices, Inc. · Model DA2000 · UDI-DI 00853569007122
10
510(k) clearances
3
Adverse events
1
Recalls
67
Facilities
Description
Dark Adaptometer
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-08-17 | Haag-Streit USA Inc | The firm recalled the device after learning of a possible deviation in the stimulus luminance of the Perimeter OCTOPUS 101. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.