GEON ELECTRONIC THERMOMETER
K-Number: K952001 · 1996-10-18
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Device Summary
Frequently Asked Questions
What is the GEON ELECTRONIC THERMOMETER?
GEON ELECTRONIC THERMOMETER is a medical device that received FDA 510(k) clearance on 1996-10-18. The listed applicant is Geon Corp.. The 510(k) number is K952001.
When did GEON ELECTRONIC THERMOMETER receive FDA 510(k) clearance?
GEON ELECTRONIC THERMOMETER received FDA 510(k) clearance on 1996-10-18, under 510(k) number K952001.
Who is the listed applicant for GEON ELECTRONIC THERMOMETER?
The FDA 510(k) record lists Geon Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GEON ELECTRONIC THERMOMETER?
The FDA product code for GEON ELECTRONIC THERMOMETER is FLL.
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 Geon Corp. 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: FLL)
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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