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FDA 510(k)

Digital Thermometer Model T103, T104

K-Number: K201879 · 2021-03-31

Decision Date2021-03-31
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Digital Thermometer Model T103, T104 is the device name listed in this FDA 510(k) record. The listed applicant is Bioland Technology, Ltd.. It received FDA 510(k) clearance on 2021-03-31 under 510(k) number K201879. 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 Digital Thermometer Model T103, T104?

Digital Thermometer Model T103, T104 is a medical device that received FDA 510(k) clearance on 2021-03-31. The listed applicant is Bioland Technology, Ltd.. The 510(k) number is K201879.

When did Digital Thermometer Model T103, T104 receive FDA 510(k) clearance?

Digital Thermometer Model T103, T104 received FDA 510(k) clearance on 2021-03-31, under 510(k) number K201879.

Who is the listed applicant for Digital Thermometer Model T103, T104?

The FDA 510(k) record lists Bioland Technology, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Digital Thermometer Model T103, T104?

The FDA product code for Digital Thermometer Model T103, T104 is FLL.

Other records listing Bioland Technology, Ltd. 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.

View all 7 devices →

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.