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Sunlight Medical, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
4
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K092554
BLASTOMERE BIOPSY PIPETTES, POLAR BODY BIOPSY PIPETTES
April 30, 2010
K072600
INTRACYTOPLASMIC SPERM AND SPERMATID INJECTION, HOLDING, ZONE DRILLING, PARTIAL ZONE DISSECTION AND
May 19, 2008