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 FASHION THERMOMETER

K-Number: K854706 · 1986-01-16

Decision Date1986-01-16
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DIGITAL FASHION THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Kanada Manufacturing Co., Ltd.. It received FDA 510(k) clearance on 1986-01-16 under 510(k) number K854706. 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 FASHION THERMOMETER?

DIGITAL FASHION THERMOMETER is a medical device that received FDA 510(k) clearance on 1986-01-16. The listed applicant is Kanada Manufacturing Co., Ltd.. The 510(k) number is K854706.

When did DIGITAL FASHION THERMOMETER receive FDA 510(k) clearance?

DIGITAL FASHION THERMOMETER received FDA 510(k) clearance on 1986-01-16, under 510(k) number K854706.

Who is the listed applicant for DIGITAL FASHION THERMOMETER?

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

What is the FDA product code for DIGITAL FASHION THERMOMETER?

The FDA product code for DIGITAL FASHION 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.

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.

↑