BONDALCAP (CARBOXYLATE)— 510(k) K801229

Substantially Equivalent

Vivadent (Usa), Inc.

FDA 510(k) clearance K801229 for BONDALCAP (CARBOXYLATE), Substantially Equivalent on 1980-06-04. Applicant: Vivadent (Usa), Inc.. Device class: 2.

Clearance details

Applicant: Vivadent (Usa), Inc.
Product code: Product code EMA
Device class: Class 2
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 1980-05-23
Decision date: 1980-06-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EMA

More clearances from Vivadent (Usa), Inc.

K863831 — VIVADENT FILPIN1986-10-14
K823409 — HELIOSIT-ORTHODONTIC1983-01-21
K813015 — HELIOSEAL1981-12-02
K802679 — SILANIT1980-12-17
K802681 — HELIOBOND1980-11-24

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