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Galaxy Intl., Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K892061 GRAND GUARD SURGICAL GLOVESKGO1989-05-23 View
510(k) K891329 STERILE PATIENT EXAMINATION GLOVESLYY1989-04-04 View
510(k) K891330 NON-STERILE PATIENT EXAMINATION GLOVESLYY1989-04-04 View
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