MODIFICATION TO POTASSIUM NITRATE-POLYCARBOXYLATE DENTAL CEMENT— 510(k) K022025

Name: FDA 510(k) clearance K022025
Creator: U.S. Food and Drug Administration
Published: 2002-08-15

Substantially Equivalent

Milton Hodosh, M.D.

FDA 510(k) clearance K022025 for MODIFICATION TO POTASSIUM NITRATE-POLYCARBOXYLATE DENTAL CEMENT, Substantially Equivalent on 2002-08-15. Applicant: Milton Hodosh, M.D.. Device class: 2.

Clearance details

Applicant: Milton Hodosh, M.D.
Product code: Code EJK
Device class: Class 2
Regulation: 21 CFR 872.3250
Advisory panel: Dental
Date received: 2002-06-20
Decision date: 2002-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Providence, RI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EJK

view all

K261728 — One-Fil LC2026-07-21
K253248 — Bright Cavity Liner2026-01-13
K230270 — 3M VitCal Liner/Base2023-02-06
K212475 — Prevest Denpro Cavity Liners (Apacal ART, Cal LC, Calcigel, CalUltra)2022-05-13
K201799 — CleaniCal2021-02-12

More clearances from Milton Hodosh, M.D.

view all

K032175 — DESENS-IONOMER2003-10-09
K031721 — COMPOSITE RESTORATION MATERIAL2003-09-11
K925207 — GLASS IONOMER CEMENT1993-07-08
K905582 — POTASSIUM NITRATE COMPOSITE RESTORATION PIT AND1991-04-29
K895988 — POTASSIUM NITRATE-ZINC OXIDE EUGENOL TEMP. DENTAL1990-03-07

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