DISINFECTION WITH THE COX DRY HEAT STERILIZER— 510(k) K910925

Name: FDA 510(k) clearance K910925
Creator: U.S. Food and Drug Administration
Published: 1992-05-08

Substantially Equivalent

Cox Sterile Products, Inc.

FDA 510(k) clearance K910925 for DISINFECTION WITH THE COX DRY HEAT STERILIZER, Substantially Equivalent on 1992-05-08. Applicant: Cox Sterile Products, Inc.. Device class: 2.

Clearance details

Applicant: Cox Sterile Products, Inc.
Product code: Code KMH
Device class: Class 2
Regulation: 21 CFR 880.6870
Advisory panel: General Hospital
Date received: 1991-03-05
Decision date: 1992-05-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KMH

view all

K094026 — STERI-DENT, STERI-SURE2011-07-12
K051660 — DENTRONIX DDS 7000 RAPID DRY HEAT STERILIZER STERILIZATION SYSTEM2005-08-04
K910202 — DENTRONIX MODEL 20001991-03-13
K880322 — DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEM1988-07-13
K881371 — COX RAPID HEAT TRANSFER STERILIZER W/12 MIN. CYCLE1988-04-13

More clearances from Cox Sterile Products, Inc.

view all

K922440 — STERIKING, SEE & PEEL1994-09-26
K872643 — COX RAPID HEAT TRANSFER STERILIZER1987-10-29

Data sourced from openFDA. This site is unofficial and independent of the FDA.