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.. Device class: 2.
Clearance details
- Applicant
- Coapt Systems, Inc.
- Product code
- Code MIX
- Device class
- Class 2
- Regulation
- 21 CFR 874.3620
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Palo Alto, CA, US
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