Map-it Diagnostic Mapping Catheters
FDA 510(k) clearance K160390 · decided 2016-04-11
Clearance details
- K-number
- K160390
- Device name
- Map-it Diagnostic Mapping Catheters
- Applicant
- Access Point Technologies Ep, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2016-02-11
- Decision date
- 2016-04-11
- Days to decision
- 60 days
- Clearance type
- Traditional
- Product code
- DRF
- Device class
- 2
- Regulation number
- 870.1220
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Rogers, MN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.