PROSTHETIC RESTORATION DEVICE— 510(k) K895283

Name: FDA 510(k) clearance K895283
Creator: U.S. Food and Drug Administration
Published: 1990-02-14

Substantially Equivalent

Swiss Precision Mfg. Corp.

FDA 510(k) clearance K895283 for PROSTHETIC RESTORATION DEVICE, Substantially Equivalent on 1990-02-14. Applicant: Swiss Precision Mfg. Corp.. Device class: 1.

Clearance details

Applicant: Swiss Precision Mfg. Corp.
Product code: Code EBL
Device class: Class 1
Regulation: 21 CFR 872.3740
Advisory panel: Dental
Date received: 1989-08-24
Decision date: 1990-02-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bayshore, NY, US

Download summary PDF View on FDA.gov ↗

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