DRI-CLAVE LIQUID KLEENZALL— 510(k) K880754

Name: FDA 510(k) clearance K880754
Creator: U.S. Food and Drug Administration
Published: 1988-05-12

Substantially Equivalent

Columbus Dental Mfg. Co.

FDA 510(k) clearance K880754 for DRI-CLAVE LIQUID KLEENZALL, Substantially Equivalent on 1988-05-12. Applicant: Columbus Dental Mfg. Co.. Device class: 1.

Clearance details

Applicant: Columbus Dental Mfg. Co.
Product code: Code EHZ
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 1988-02-25
Decision date: 1988-05-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EHZ

view all

K973248 — IMTEC BONE COLLECTOR SYSTEM1997-11-19
K941164 — TAP EXPRESS EJECTOR1994-05-18
K911072 — SUPER EVACRETRACTOR, DISPOSABLE ORAL EVACUATOR1991-05-15
K903718 — OROSCOPE MODEL NUMBER COS-1001990-11-09
K892881 — DENTAL SANI-SLEEVE STERILE 60MM X 1650MM #11011989-06-23

More clearances from Columbus Dental Mfg. Co.

view all

K880607 — UTILITY WAX STRIPS, SPEARMINT1988-03-31
K880606 — UTILITY WAX STRIPS, CINNAMON1988-03-24
K872243 — PEKALUX(TM)1987-07-07
K871164 — GLUMA(TM) BONDING SYSTEM1987-07-02
K872272 — PEKALUX/GLUMA LIGHT CURED ANTERIOR RESTORATIVE SYS1987-07-02

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