FDA Device Intelligence
Home › MEDICAPTURE, INC. › MTS

MTS

MEDICAPTURE, INC. · Model MTS156 · UDI-DI 00859151005057

FWH
2
510(k) clearances
12
Adverse events
1
Recalls
2
Facilities

Description

Monitor with Touch Screen

Recalls

DateFirmReason
2012-07-10Berchtold Corp.Defective camera: There is a possibility that the connection of the wires to the connector may become loose, causing image distortion or loss.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.