REUMA TEST— 510(k) K873782

Substantially Equivalent

Sclavo, Inc.

FDA 510(k) clearance K873782 for REUMA TEST, Substantially Equivalent on 1987-11-27. Applicant: Sclavo, Inc.. Device class: 2.

Clearance details

Applicant: Sclavo, Inc.
Product code: Code DHR
Device class: Class 2
Regulation: 21 CFR 866.5775
Advisory panel: Immunology
Date received: 1987-09-16
Decision date: 1987-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wayne, NJ, 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.