EYE SPOT RF TEST— 510(k) K932437

Substantially Equivalent

J & S Medical Assoc., Inc.

FDA 510(k) clearance K932437 for EYE SPOT RF TEST, Substantially Equivalent on 1993-08-23. Applicant: J & S Medical Assoc., Inc.. Device class: 2.

Clearance details

Applicant: J & S Medical Assoc., Inc.
Product code: Code DHR
Device class: Class 2
Regulation: 21 CFR 866.5775
Advisory panel: Immunology
Date received: 1993-05-19
Decision date: 1993-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Natick, MA, 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.