RHYTHMLINK DISPOSABLE CONCENTRIC STIMULATING PROBE— 510(k) K132138
Substantially EquivalentRhythmlink International, LLC
FDA 510(k) clearance K132138 for RHYTHMLINK DISPOSABLE CONCENTRIC STIMULATING PROBE, Substantially Equivalent on 2014-04-11. Applicant: Rhythmlink International, LLC. Device class: 2.
Clearance details
- Applicant
- Rhythmlink International, LLC
- Product code
- Code PDQ
- Device class
- Class 2
- Regulation
- 21 CFR 874.1820
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Columbia, SC, US
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