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Martin S. Knopf Assoc., Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K942214 H55 HYDROPHILIC CONTACT LENSLPL1994-07-28 View
510(k) K910532 URAM OPHTHALMIC LASER ENDOSCOPEHQF1991-05-28 View
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