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Engineering, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K881521
MODIFIED SERVO SYRINGE
May 31, 1988
K862749
LS9000 SUCTION BIOPSY NEEDLE
September 15, 1986
K862476
LS3000 CANNULA UTERINE SUCTION
July 18, 1986
K854359
LM2000A SURGICAL SUCTION MONITOR
March 3, 1986
K854844
LS1000 SURGICAL ASPIRATOR II
February 12, 1986