num Vapocoolant
FDA 510(k) clearance K202782 · decided 2020-12-21
Clearance details
- K-number
- K202782
- Device name
- num Vapocoolant
- Applicant
- 623 Medical, LLC
- Decision
- Substantially Equivalent
- Date received
- 2020-09-22
- Decision date
- 2020-12-21
- Days to decision
- 90 days
- Clearance type
- Traditional
- Product code
- MLY
- Device class
- U
- Medical specialty
- Unknown
- Advisory committee
- Unknown
- Location
- Morrisville, NC, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.