FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇭 Switzerland
PROWLER SELECT PLUS; PROWLER EX
K Number: K210838
·
Decision Aug 25, 2021
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
174
Applicant Total
96
Review Days
156
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Basic Information
- Device Name
- PROWLER SELECT PLUS; PROWLER EX
- K Number
- K210838
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.1210
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medos International SARL
- Date Received
- March 22, 2021
- Decision Date
- August 25, 2021
- Product Code
- KRA
- 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 |
|---|---|---|---|
| KRA | Catheter, Continuous Flush | FDA class 2 | Cardiovascular |
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