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Hart Enterprises, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K921683 PENCIL POINT SPINAL NEEDLEBSP1993-08-26 View
510(k) K913815 AUTOMATED BIOPSY DEVICE, MODIFICATIONDWO1991-10-30 View
510(k) K885149 NEEDLE INSERT FOR SOFT TISSUE BIOPSY DEVICEDWO1989-01-26 View
510(k) K881730 BREAST LOCALIZATION NEEDLESGDM1988-05-13 View
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