DeviceClearance

QUANTIX/OR BLOOD FLOW MONITOR; FLEXIBLE PROBE WITH OPTIONAL VESSEL STABILIZER— 510(k) K050088

Substantially Equivalent

Neoprobe Corp.

FDA 510(k) clearance K050088 for QUANTIX/OR BLOOD FLOW MONITOR; FLEXIBLE PROBE WITH OPTIONAL VESSEL STABILIZER, Substantially Equivalent on 2005-02-08. Applicant: Neoprobe Corp.. Device class: 2.

Clearance details

Applicant
Neoprobe Corp.
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
Special
Location
Dublin, OH, US
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