DISPOSABLE PROBE FOR AQUAMATIC K-THERMIA
K-Number: K810747 · 1981-03-19
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE PROBE FOR AQUAMATIC K-THERMIA?
DISPOSABLE PROBE FOR AQUAMATIC K-THERMIA is a medical device that received FDA 510(k) clearance on 1981-03-19. The listed applicant is American Hamilton. The 510(k) number is K810747.
When did DISPOSABLE PROBE FOR AQUAMATIC K-THERMIA receive FDA 510(k) clearance?
DISPOSABLE PROBE FOR AQUAMATIC K-THERMIA received FDA 510(k) clearance on 1981-03-19, under 510(k) number K810747.
Who is the listed applicant for DISPOSABLE PROBE FOR AQUAMATIC K-THERMIA?
The FDA 510(k) record lists American Hamilton as the applicant. This does not by itself establish the device manufacturer.
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 American Hamilton 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.
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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