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FDA 510(k)

AMSINO CLINICAL THERMOMETER

K-Number: K960185 · 1996-03-28

Decision Date1996-03-28
Product CodeFLK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AMSINO CLINICAL THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Amsia Intl., Inc.. It received FDA 510(k) clearance on 1996-03-28 under 510(k) number K960185. The device is classified under product code FLK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMSINO CLINICAL THERMOMETER?

AMSINO CLINICAL THERMOMETER is a medical device that received FDA 510(k) clearance on 1996-03-28. The listed applicant is Amsia Intl., Inc.. The 510(k) number is K960185.

When did AMSINO CLINICAL THERMOMETER receive FDA 510(k) clearance?

AMSINO CLINICAL THERMOMETER received FDA 510(k) clearance on 1996-03-28, under 510(k) number K960185.

Who is the listed applicant for AMSINO CLINICAL THERMOMETER?

The FDA 510(k) record lists Amsia Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMSINO CLINICAL THERMOMETER?

The FDA product code for AMSINO 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 Amsia Intl., 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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