FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Guiding Catheter
K Number: K210009
·
Decision Nov 24, 2021
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
13
Review Days
324
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Basic Information
- Device Name
- Guiding Catheter
- K Number
- K210009
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1250
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- CenterPoint Systems, LLC
- Date Received
- January 4, 2021
- Decision Date
- November 24, 2021
- Product Code
- DQY
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| DQY | Catheter, Percutaneous | FDA class 2 | Cardiovascular |
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|---|---|---|---|
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