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Introspect, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K951255
IMEDGE VIDEO OSTOSCOPE (ANALOG)
April 13, 1995
K950983
IMEDGE DIGITA OTOSCOPE OR DIGITAL VIDEO OTOSCOPE
April 12, 1995