FDA 510(k)
FDA class 2
Substantially Equivalent
🇬🇧 United Kingdom
DoubleChek DC-1001
K Number: K212316
·
Decision Sep 30, 2022
Classifications
1
FEI Numbers
242
Registration Numbers
243
Same Product Code
648
Applicant Total
1
Review Days
431
Basic Information
- Device Name
- DoubleChek DC-1001
- K Number
- K212316
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5980
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Nasogastric Feeding Solutions, Ltd.
- Date Received
- July 26, 2021
- Decision Date
- September 30, 2022
- Product Code
- KNT
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- GU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| KNT | Tubes, Gastrointestinal (And Accessories) | FDA class 2 | Gastroenterology, Urology |
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