FEVER TESTER
K-Number: K790532 · 1979-05-29
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Device Summary
Frequently Asked Questions
What is the FEVER TESTER?
FEVER TESTER is a medical device that received FDA 510(k) clearance on 1979-05-29. The listed applicant is Maddak, Inc.. The 510(k) number is K790532.
When did FEVER TESTER receive FDA 510(k) clearance?
FEVER TESTER received FDA 510(k) clearance on 1979-05-29, under 510(k) number K790532.
Who is the listed applicant for FEVER TESTER?
The FDA 510(k) record lists Maddak, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FEVER TESTER?
The FDA product code for FEVER TESTER is KPD.
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 Maddak, 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: KPD)
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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