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Intubation Guide Kit

Nar Medical Depot, LLC · Model 800-00046 · UDI-DI 00860009615533

OGK
0
510(k) clearances
3
Adverse events
2
Recalls
13
Facilities

Description

AIR Q KIT - SZ 3

Recalls

DateFirmReason
2021-08-04Smiths Medical ASD Inc.The incorrect device is contained in the package.
2012-06-18superDimension, IncsuperDimension, Inc., is conducting a recall of certain superDimension Systems operating Software Version 4.0 - 4.9. The affected systems are sold under the product code AAS00016-

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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.