BIOLASTIC SUPER ELASTIC ARCHES— 510(k) K902050

Substantially Equivalent

Rmo, Inc.

FDA 510(k) clearance K902050 for BIOLASTIC SUPER ELASTIC ARCHES, Substantially Equivalent on 1990-08-03. Applicant: Rmo, Inc.. Device class: 1.

Clearance details

Applicant: Rmo, Inc.
Product code: Code EJF
Device class: Class 1
Regulation: 21 CFR 872.5410
Advisory panel: Dental
Date received: 1990-05-07
Decision date: 1990-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denver, CO, US

Download summary PDF View on FDA.gov ↗

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K933080 — ORTHOTECH DURA-GOLD BARCKETS1994-03-23

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