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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K093889

MODIFICATION TO: HG III ULTRA WIDE SYSTEM · Hiossen, Inc. · decided 2010-04-22 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
HG III Ultra-Wide Fixture RBM Pre-MountedAHG3S6013RHIOSSEN, INC.DZE00814913022123
HG III Ultra-Wide Fixture RBM Pre-MountedAHG3S7011RHIOSSEN, INC.DZE00814913022161
HG III Ultra-Wide Fixture RBM Pre-MountedAHG3S6007RHIOSSEN, INC.DZE00814913022086
HG III Ultra-Wide Fixture RBM Pre-MountedAHG3S7013RHIOSSEN, INC.DZE00814913022178
HG III Ultra-Wide Fixture RBM Pre-MountedAHG3S7007RHIOSSEN, INC.DZE00814913022130
HG III Ultra-Wide Fixture RBM Pre-MountedAHG3S6010RHIOSSEN, INC.DZE00814913022109
HG III Ultra-Wide Fixture RBM Pre-MountedAHG3S7010RHIOSSEN, INC.DZE00814913022154
HG III Ultra-Wide Fixture RBM Pre-MountedAHG3S7008RHIOSSEN, INC.DZE00814913022147
HG III Ultra-Wide Fixture RBM Pre-MountedAHG3S6008RHIOSSEN, INC.DZE00814913022093
HG III Ultra-Wide Fixture RBM Pre-MountedAHG3S6011RHIOSSEN, INC.DZE00814913022116