DeviceClearance

VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger— 510(k) K211589

Substantially Equivalent

Remington Medical, Inc.

FDA 510(k) clearance K211589 for VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger, Substantially Equivalent on 2022-01-27. Applicant: Remington Medical, Inc..

Clearance details

Applicant
Remington Medical, Inc.
Product code
Code DPW
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Alpharetta, GA, US
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.