LIQUA-SONIC GEL— 510(k) K841871
Substantially EquivalentChester Labs, Inc.
FDA 510(k) clearance K841871 for LIQUA-SONIC GEL, Substantially Equivalent on 1985-03-14. Applicant: Chester Labs, Inc.. Device class: 2.
Clearance details
- Applicant
- Chester Labs, Inc.
- Product code
- Code GYB
- Device class
- Class 2
- Regulation
- 21 CFR 882.1275
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Erlanger, KY, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.