Medical Device Manufacturer · US , Dallas , TX

Cox Sterile Products, Inc.

4 submissions · 4 cleared · Since 1987

Total

Cleared

Denied

Cox Sterile Products, Inc. — FDA 510(k) Submissions

Cox Sterile Products, Inc. has submitted 4 FDA 510(k) premarket notifications since 1987, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Sterilizer, Dry Heat, Sterilization Wrap Containers, Trays, Cassettes & Other Accessories . Use the specialty filter in the sidebar to narrow results.

4 devices

1–4 of 4

STERIKING, SEE & PEEL

K922440 · KCT Sterilization Wrap... · General Hospital

Sep 1994 857d

DISINFECTION WITH THE COX DRY HEAT STERILIZER

K910925 · KMH Sterilizer, Dry Heat · General Hospital

May 1992 430d

COX RAPID HEAT TRANSFER STERILIZER W/12 MIN. CYCLE

K881371 · KMH Sterilizer, Dry Heat · General Hospital

Apr 1988 12d

COX RAPID HEAT TRANSFER STERILIZER

K872643 · KMH Sterilizer, Dry Heat · General Hospital

Oct 1987 115d

Data Source

FDA 510(k) public files . 174,402 total devices indexed.

Cox Sterile Products, Inc.

Cox Sterile Products, Inc. — FDA 510(k) Submissions

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