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FDA 510(k)

AVITA AGIL IT 101 INSTANT DIGITAL THERMOMETER

K-Number: K012136 · 2001-09-10

Decision Date2001-09-10
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AVITA AGIL IT 101 INSTANT DIGITAL THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Avita Corporation. It received FDA 510(k) clearance on 2001-09-10 under 510(k) number K012136. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AVITA AGIL IT 101 INSTANT DIGITAL THERMOMETER?

AVITA AGIL IT 101 INSTANT DIGITAL THERMOMETER is a medical device that received FDA 510(k) clearance on 2001-09-10. The listed applicant is Avita Corporation. The 510(k) number is K012136.

When did AVITA AGIL IT 101 INSTANT DIGITAL THERMOMETER receive FDA 510(k) clearance?

AVITA AGIL IT 101 INSTANT DIGITAL THERMOMETER received FDA 510(k) clearance on 2001-09-10, under 510(k) number K012136.

Who is the listed applicant for AVITA AGIL IT 101 INSTANT DIGITAL THERMOMETER?

The FDA 510(k) record lists Avita Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AVITA AGIL IT 101 INSTANT DIGITAL THERMOMETER?

The FDA product code for AVITA AGIL IT 101 INSTANT DIGITAL 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 Avita Corporation 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.

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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

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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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