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FDA Product Code

FDA Product Code KMH — Clearance Directory

Device Class
Class II
Assigned Panel
General Hospital
21 CFR Citation
880.6870

510(k) Clearances — 10 records

K-Number Device Name Applicant Decision Date Clearance Type Summary
K094026 STERI-DENT, STERI-SURE Cpac, Inc. 2011-07-12 Traditional PDF ↗
K051660 DENTRONIX DDS 7000 RAPID DRY HEAT STERILIZER STERILIZATION SYSTEM Coltene/Whaledent, Inc. 2005-08-04 Traditional PDF ↗
K910925 DISINFECTION WITH THE COX DRY HEAT STERILIZER Cox Sterile Products, Inc. 1992-05-08 Traditional PDF ↗
K910202 DENTRONIX MODEL 2000 Dentronix, Inc. 1991-03-13 Traditional PDF ↗
K880322 DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEM Dentronix, Inc. 1988-07-13 Traditional PDF ↗
K881371 COX RAPID HEAT TRANSFER STERILIZER W/12 MIN. CYCLE Cox Sterile Products, Inc. 1988-04-13 Traditional PDF ↗
K872643 COX RAPID HEAT TRANSFER STERILIZER Cox Sterile Products, Inc. 1987-10-29 Traditional PDF ↗
K871615 U. V. GERMICIDAL UNIT Lorvic Corp. 1987-09-11 Traditional PDF ↗
K851307 INOX DRY HEAT STERILIZER Broadwest Corp. 1985-05-09 Traditional PDF ↗
K771070 DRY HEAT STERILIZER Cpac, Inc. 1977-07-14 Traditional PDF ↗

Product code KMH · Class II · General Hospital. Data: openFDA.