Medical Device Manufacturer · US , Elgin , IL

Hydrox Laboratories

2 submissions · 2 cleared · Since 1998

Total

Cleared

Denied

Hydrox Laboratories — FDA 510(k) Submissions

Hydrox Laboratories has submitted 2 FDA 510(k) premarket notifications since 1998, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter And Tip, Suction . Use the specialty filter in the sidebar to narrow results.

2 devices

1–2 of 2

HYDROX STERILE WATER 4 OZ. CUP 120 ML., HYDROX STERILE WATER 100 ML BOTTLE

K974758 · JOL Catheter And Tip, Suction · General Hospital

Mar 1998 80d

HYDROX SALINE SOLUTION 0.9% SODIUM CHLORIDE 4 OZ. CUP 120 ML 100 ML BOTTLE

K974759 · JOL Catheter And Tip, Suction · General Hospital

Mar 1998 80d

Hydrox Laboratories

Hydrox Laboratories — FDA 510(k) Submissions

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