Apollo Balloon Dilatation Catheter
FDA 510(k) clearance K153742 · decided 2016-08-08
Clearance details
- K-number
- K153742
- Device name
- Apollo Balloon Dilatation Catheter
- Applicant
- Brosmed Medical Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2015-12-28
- Decision date
- 2016-08-08
- Days to decision
- 224 days
- Clearance type
- Traditional
- Product code
- LOX
- Device class
- 2
- Regulation number
- 870.5100
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Dongguan, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.