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Dsp Worldwide
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K962544
MICRO DIAMOND-POINT DISSECTION NEEDLES
September 20, 1996
K962371
DERMTOME BLADE
August 29, 1996
K962365
XENON LIGHTSOURCE
July 18, 1996