VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger— 510(k) K212065
Substantially EquivalentRemington Medical, Inc.
FDA 510(k) clearance K212065 for VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger, Substantially Equivalent on 2021-10-07. Applicant: Remington Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Remington Medical, Inc.
- 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
- Alpharetta, GA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.