FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BENCHMARK BMX81 Access System
K Number: K221822
·
Decision Nov 4, 2022
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
91
Applicant Total
87
Review Days
134
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Basic Information
- Device Name
- BENCHMARK BMX81 Access System
- K Number
- K221822
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1250
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Penumbra, Inc.
- Date Received
- June 23, 2022
- Decision Date
- November 4, 2022
- Product Code
- QJP
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| QJP | Catheter, Percutaneous, Neurovasculature | FDA class 2 | Cardiovascular |
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