VISI-SPOT— 510(k) K932752

Substantially Equivalent

J.S. Medical Assoc.

FDA 510(k) clearance K932752 for VISI-SPOT, Substantially Equivalent on 1993-11-05. Applicant: J.S. Medical Assoc.. Device class: 1.

Clearance details

Applicant: J.S. Medical Assoc.
Product code: Code JTO
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1993-05-19
Decision date: 1993-11-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Natick, MA, US

Download summary PDF View on FDA.gov ↗

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K924247 — ACCUTEX ASO LATEX TEST1992-12-07

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