Recall Z-1693-2023— p-Chip Corporation
Class II · Ongoing
Class II FDA medical device recall by p-Chip Corporation, initiated 2021-03-03. FDA's recall record names no specific 510(k) clearance for this event. Product: p-Chip Wand Reader. Reason: The laser operation might fall under a higher laser class..
- Recalling firm
- p-Chip Corporation
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2021-03-03
- Firm location
- Chicago, IL, United States
Product description
p-Chip Wand Reader
Reason for recall
The laser operation might fall under a higher laser class.
Data sourced from openFDA. This site is unofficial and independent of the FDA.