GERATHERM MERCUIRY FREE CLINICAL THERMOMETER
K-Number: K960224 · 1996-03-25
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Device Summary
Frequently Asked Questions
What is the GERATHERM MERCUIRY FREE CLINICAL THERMOMETER?
GERATHERM MERCUIRY FREE CLINICAL THERMOMETER is a medical device that received FDA 510(k) clearance on 1996-03-25. The listed applicant is Rg Ent., Inc.. The 510(k) number is K960224.
When did GERATHERM MERCUIRY FREE CLINICAL THERMOMETER receive FDA 510(k) clearance?
GERATHERM MERCUIRY FREE CLINICAL THERMOMETER received FDA 510(k) clearance on 1996-03-25, under 510(k) number K960224.
Who is the listed applicant for GERATHERM MERCUIRY FREE CLINICAL THERMOMETER?
The FDA 510(k) record lists Rg Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GERATHERM MERCUIRY FREE CLINICAL THERMOMETER?
The FDA product code for GERATHERM MERCUIRY FREE CLINICAL THERMOMETER is FLK.
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 Rg Ent., 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: FLK)
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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