FloPatch FP120— 510(k) K223843
Substantially EquivalentFlosonics Medical
FDA 510(k) clearance K223843 for FloPatch FP120, Substantially Equivalent on 2023-05-03. Applicant: Flosonics Medical. Device class: 2.
Clearance details
- Applicant
- Flosonics Medical
- Product code
- Code DPW
- Device class
- Class 2
- Regulation
- 21 CFR 870.2100
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Toronto, CA
Recent devices under product code DPW
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view allRecalls naming K223843
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K223843.
Data sourced from openFDA. This site is unofficial and independent of the FDA.