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Devices · ICAD, INC.

SECOND LOOK ™

PMAP010034RadiologyMYN

ICAD, INC. is listed for SECOND LOOK ™ (P010034). The FDA list gives January 31, 2002 as the date of the final decision. The lead panel is Radiology, and the database link on the FDA list is the PMA pathway. openFDA describes product code MYN as “Analyzer, Medical Image”: For information on the MYN device, please see: https://www.federalregister.gov/documents/2020/01/22/2020-00494/radiology-devices-reclassification-of-medical-image-analyzers openFDA records decision code APWD for this submission. This paragraph is assembled only from those public fields. It is not an FDA review, not a determination of safety or effectiveness, and not medical advice. Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=P010034

Official FDA database record

Date of final decision
January 31, 2002
Company on the FDA list
ICAD, INC.
Lead panel
Radiology
Primary product code
MYN
openFDA device name for the code
Analyzer, Medical Image
Device class
2
Regulation number
892.2070
openFDA decision description
Not returned
openFDA decision code
APWD
Statement or summary label
Statement

Product-code text from openFDA

For information on the MYN device, please see: https://www.federalregister.gov/documents/2020/01/22/2020-00494/radiology-devices-reclassification-of-medical-image-analyzers