CASTLE PROCEDURE AND RITTER EXAM. TABLES— 510(k) K810900

Name: FDA 510(k) clearance K810900
Creator: U.S. Food and Drug Administration
Published: 1981-04-21

Substantially Equivalent

Sybron Corp.

FDA 510(k) clearance K810900 for CASTLE PROCEDURE AND RITTER EXAM. TABLES, Substantially Equivalent on 1981-04-21. Applicant: Sybron Corp.. Device class: 1.

Clearance details

Applicant: Sybron Corp.
Product code: Code LGX
Device class: Class 1
Regulation: 21 CFR 878.4960
Advisory panel: General, Plastic Surgery
Date received: 1981-04-03
Decision date: 1981-04-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.