Atlas FDA

MLC

2 FDA 510(k) clearances · Product code

FDA profile

Official device name
Monitor, St Segment
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2340
Medical specialty
Cardiovascular
Flags
Third-party review eligible
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RecordFirmDate
NARKOMED 6000 (K993826)Draeger Medical, Inc.2000-03-23
DATASCOPE 6000 MONITOR (K926099)Datascope Corp.1993-08-06

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Every clearance here is in the API, with alerts when new ones post.