VF LIQUIGEL— 510(k) K083783
Substantially EquivalentCoapt Systems, Inc.
FDA 510(k) clearance K083783 for VF LIQUIGEL, Substantially Equivalent on 2009-09-11. Applicant: Coapt Systems, Inc..
Clearance details
- Applicant
- Coapt Systems, Inc.
- Product code
- Code MIX
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Palo Alto, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.