Atlas FDA

JIM

2 FDA 510(k) clearances · Product code

FDA profile

Official device name
Method, Metallic Reduction, Glucose (Urinary, Non-Quantitative)
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1340
Medical specialty
Clinical Chemistry
Flags
Third-party review eligible
Adverse events (MAUDE)
2001: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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RecordFirmDate
HI CHEM ISE REAGENTS (PRODUCTS #88960 AND #88964) (K902155)Hichem Diagnostics1990-06-12
CHEMTAB (K790772)Boehringer Mannheim Corp.1979-06-15

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