FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Kodiak Dual Port Coaxial Introducer Kit
K Number: K230631
·
Decision May 22, 2023
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
5
Review Days
76
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Basic Information
- Device Name
- Kodiak Dual Port Coaxial Introducer Kit
- K Number
- K230631
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1340
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Argon Medical Devices
- Date Received
- March 7, 2023
- Decision Date
- May 22, 2023
- Product Code
- DYB
- 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 |
|---|---|---|---|
| DYB | Introducer, Catheter | FDA class 2 | Cardiovascular |
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