FDA Import Refusal 508-0381213-5/131/1 — Lake Region Manufacturing, Inc
The FDA refused shipment 508-0381213-5/131/1 from Lake Region Manufacturing, Inc (United States) on Jun 3, 2019. The refused product falls under Devices — CATHETER, CAROTID, TEMPORARY, FOR EMBOLIZATION CAPTURE. Cited charge: 341
Refusal Details
- Date
- Jun 3, 2019
- Country
- United States
- Product Category
- Devices
- Product Code
- 74NTE CATHETER, CAROTID, TEMPORARY, FOR EMBOLIZATION CAPTURE
- Charges
- 341