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Sis Ltd., Surgical Instrument Systems

FDA Regulatory Profile

Sis Ltd., Surgical Instrument Systems appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 9, 2009.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Known Names

sis ltd. surgical instrument systems, sis ltd., surgical instrument systems

Recent 510(k) Clearances

K-NumberDeviceDate
K082871XACT LENS INSERTER SYSTEM, MODELS 6MM, 7MMJuly 9, 2009
K051940CM 3910 ROTATING DOUBLE SCHEIMPFLUG CAMERASeptember 28, 2005
K043150AMADEUS II EPIKERATOMEJanuary 31, 2005

FDA data resources