MERCURY THERMOMETERS (ORAL AND RECTAL)
K-Number: K900646 · 1990-07-11
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Device Summary
Frequently Asked Questions
What is the MERCURY THERMOMETERS (ORAL AND RECTAL)?
MERCURY THERMOMETERS (ORAL AND RECTAL) is a medical device that received FDA 510(k) clearance on 1990-07-11. The listed applicant is Abel Industries, Inc.. The 510(k) number is K900646.
When did MERCURY THERMOMETERS (ORAL AND RECTAL) receive FDA 510(k) clearance?
MERCURY THERMOMETERS (ORAL AND RECTAL) received FDA 510(k) clearance on 1990-07-11, under 510(k) number K900646.
Who is the listed applicant for MERCURY THERMOMETERS (ORAL AND RECTAL)?
The FDA 510(k) record lists Abel Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MERCURY THERMOMETERS (ORAL AND RECTAL)?
The FDA product code for MERCURY THERMOMETERS (ORAL AND RECTAL) 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.
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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