Atlas FDA

ONGUARD

FDA premarket approval P000041/S009 · decided 2010-06-10

Approval details

PMA number
P000041
Supplement
S009
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
ONGUARD
Generic name
Analyzer, medical image
Applicant
Riverain Medical Group
Date received
2009-12-10
Decision date
2010-06-10
Days to decision
182 days
Decision code
APPR
Product code
MYN
Advisory committee
Radiology
Expedited review
No
Location
Miamisburg, OH
Statement
APPROVAL FOR THE ONGUARD 5.1 CADE SOFTWARE.

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510(k) clearances by this applicant

RecordFirmDate
SOFTVIEW, MODEL 2.01 (K092363)Riverain Medical Group2010-03-18