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)

Phoenix Digital Thermometer

K-Number: K201032 · 2021-10-29

Decision Date2021-10-29
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Phoenix Digital Thermometer is the device name listed in this FDA 510(k) record. The listed applicant is Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.. It received FDA 510(k) clearance on 2021-10-29 under 510(k) number K201032. 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 Phoenix Digital Thermometer?

Phoenix Digital Thermometer is a medical device that received FDA 510(k) clearance on 2021-10-29. The listed applicant is Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.. The 510(k) number is K201032.

When did Phoenix Digital Thermometer receive FDA 510(k) clearance?

Phoenix Digital Thermometer received FDA 510(k) clearance on 2021-10-29, under 510(k) number K201032.

Who is the listed applicant for Phoenix Digital Thermometer?

The FDA 510(k) record lists Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Phoenix Digital Thermometer?

The FDA product code for Phoenix Digital Thermometer is FLL.

Other records listing Phoenix Innovative Healthcare Manufacturers Pvt. , 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.