GRAM NEGATIVE FLUORESCENT IDENTIFICATION PANEL— 510(k) K862642

Name: FDA 510(k) clearance K862642
Creator: U.S. Food and Drug Administration
Published: 1986-09-11

Substantially Equivalent

American Micro Scan

FDA 510(k) clearance K862642 for GRAM NEGATIVE FLUORESCENT IDENTIFICATION PANEL, Substantially Equivalent on 1986-09-11. Applicant: American Micro Scan. Device class: 1.

Clearance details

Applicant: American Micro Scan
Product code: Code LQM
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1986-07-11
Decision date: 1986-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Sacramento, CA, US

Download summary PDF View on FDA.gov ↗

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