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The Sanborn Co.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K901553 SURG-K SURGICAL KERATOMETERHLR1990-07-20 View
510(k) K901523 VKG 1000, VIDEO KERATOGRAPHHJA1990-06-27 View
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