VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger— 510(k) K212065

Substantially Equivalent

Remington 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..

Clearance details

Applicant: Remington Medical, Inc.
Product code: Code DPW
Advisory panel: Cardiovascular
Date received: 2021-07-02
Decision date: 2021-10-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alpharetta, GA, US

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