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FDA 510(k)

TEMP-A-SURE

K-Number: K010866 · 2001-06-06

Decision Date2001-06-06
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TEMP-A-SURE is the device name listed in this FDA 510(k) record. The listed applicant is Homecare Technologies , Ltd.. It received FDA 510(k) clearance on 2001-06-06 under 510(k) number K010866. 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 TEMP-A-SURE?

TEMP-A-SURE is a medical device that received FDA 510(k) clearance on 2001-06-06. The listed applicant is Homecare Technologies , Ltd.. The 510(k) number is K010866.

When did TEMP-A-SURE receive FDA 510(k) clearance?

TEMP-A-SURE received FDA 510(k) clearance on 2001-06-06, under 510(k) number K010866.

Who is the listed applicant for TEMP-A-SURE?

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

What is the FDA product code for TEMP-A-SURE?

The FDA product code for TEMP-A-SURE is FLL.

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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