MOSES Raydar™

Boston Scientific Corporation

Country / region:United States (US)Submission type:Traditional

Product code GEX· 21 CFR 878.4810

Company

United States (US)

Product code

GEX
21 CFR 878.4810

Predicate devices

0
Cited in this 510(k)

Cited as predicate

0

Device details

FDA 510(k) registration fields

K number
K260100
Device name
MOSES Raydar™
Country / region
United States(US)
Product code
GEX
Device class
Class 2
Regulation number
21 CFR 878.4810
Date received
2026-01-13
Decision date
2026-05-18
Submission type
Traditional

Predicate devices

0

No predicate K numbers were extracted

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Cited as predicate

0

No later 510(k)s cite this device yet

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