Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DIGITAL THERMOMETER CLASSIC TYPE AND FLEXIBLE TYPE

K-Number: K023711 · 2002-11-21

Decision Date2002-11-21
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DIGITAL THERMOMETER CLASSIC TYPE AND FLEXIBLE TYPE is the device name listed in this FDA 510(k) record. The listed applicant is Acute Ideas Co. , Ltd.. It received FDA 510(k) clearance on 2002-11-21 under 510(k) number K023711. 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 CLASSIC TYPE AND FLEXIBLE TYPE?

DIGITAL THERMOMETER CLASSIC TYPE AND FLEXIBLE TYPE is a medical device that received FDA 510(k) clearance on 2002-11-21. The listed applicant is Acute Ideas Co. , Ltd.. The 510(k) number is K023711.

When did DIGITAL THERMOMETER CLASSIC TYPE AND FLEXIBLE TYPE receive FDA 510(k) clearance?

DIGITAL THERMOMETER CLASSIC TYPE AND FLEXIBLE TYPE received FDA 510(k) clearance on 2002-11-21, under 510(k) number K023711.

Who is the listed applicant for DIGITAL THERMOMETER CLASSIC TYPE AND FLEXIBLE TYPE?

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

What is the FDA product code for DIGITAL THERMOMETER CLASSIC TYPE AND FLEXIBLE TYPE?

The FDA product code for DIGITAL THERMOMETER CLASSIC TYPE AND FLEXIBLE TYPE 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 Acute Ideas Co. , 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.

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

View on FDA Database →

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

↑