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Noetix, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K893992
NOETIX, BIOPSY NEEDLE
September 8, 1989
K881635
NOETIX(R) SURGICAL EXTRACTION(TM) SYSTEM
July 1, 1988
K871365
CAPSULECTOMER CYSTOTOME
April 16, 1987