KOH MOUNTING FLUID W/GLYCEROL
K-Number: K792709 · 1980-01-24
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Device Summary
Frequently Asked Questions
What is the KOH MOUNTING FLUID W/GLYCEROL?
KOH MOUNTING FLUID W/GLYCEROL is a medical device that received FDA 510(k) clearance on 1980-01-24. The listed applicant is Meridian Diagnostics, Inc.. The 510(k) number is K792709.
When did KOH MOUNTING FLUID W/GLYCEROL receive FDA 510(k) clearance?
KOH MOUNTING FLUID W/GLYCEROL received FDA 510(k) clearance on 1980-01-24, under 510(k) number K792709.
Who is the listed applicant for KOH MOUNTING FLUID W/GLYCEROL?
The FDA 510(k) record lists Meridian Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KOH MOUNTING FLUID W/GLYCEROL?
The FDA product code for KOH MOUNTING FLUID W/GLYCEROL is KEQ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Meridian Diagnostics, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KEQ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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