Canon Inc.
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Canon Full Auto Ref-Keratometer RK-F2, Catalog Number 6937B002AA. Product Usage: This devi recall (Z-1404-2013) | Canon Inc. | 2013-05-25 |
| Canon Solid State X-ray Imager (Flat Panel/Digital Imager), Digital Radiography, Models CX recall (Z-2265-2012) | Canon Inc. | 2012-08-24 |
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Every clearance here is in the API, with alerts when new ones post.