FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DiLumen C2 and Tool Mount
K Number: K211819
·
Decision Oct 22, 2021
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
108
Applicant Total
8
Review Days
133
Basic Information
- Device Name
- DiLumen C2 and Tool Mount
- K Number
- K211819
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.1500
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Lumendi, LLC
- Date Received
- June 11, 2021
- Decision Date
- October 22, 2021
- Product Code
- FDF
- 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 |
|---|---|---|---|
| FDF | Colonoscope And Accessories, Flexible/Rigid | FDA class 2 | Gastroenterology, Urology |
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Other Clearances by Lumendi, LLC
| K Number | Device Name | ||
|---|---|---|---|
| K221452 | DiLumen C1, EZ1 and Tool Mount | Feb 10, 2023 | Substantially Equivalent |
| K210851 | DiLumen Endolumenal Interventional Platform (DiLumen) | Apr 21, 2021 | Substantially Equivalent |
| K183112 | DiLumen Endolumenal Interventional Knife (DiLumen IK) | Aug 2, 2019 | Substantially Equivalent |
| K182540 | DiLumen Endolumenal Interventional Platform | Oct 30, 2018 | Substantially Equivalent |
| K173405 | DiLumen Endolumenal Interventional Scissors (DiLumen Is) | May 22, 2018 | Substantially Equivalent |
| K173317 | DiLumen C2; DiLumen Tool Mount | Apr 17, 2018 | Substantially Equivalent |
| K162428 | DiLumen Endolumenal Interventional Platform | Dec 6, 2016 | Substantially Equivalent |