ViewFlex Xtra Reprocessed ICE Catheter— 510(k) K222217
Substantially EquivalentABBOTT MEDICAL
FDA 510(k) clearance K222217 for ViewFlex Xtra Reprocessed ICE Catheter, Substantially Equivalent on 2022-12-19. Applicant: ABBOTT MEDICAL. Device class: 2.
Clearance details
- Applicant
- ABBOTT MEDICAL
- Product code
- Product code OWQ
- Device class
- Class 2
- Regulation
- 21 CFR 870.1200
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minnetonka, MN, US
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More clearances from ABBOTT MEDICAL
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