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)

TEMPO2-I DISPOSABLE THERMOMETERS

K-Number: K790890 · 1979-06-27

ApplicantAirlife, Inc.
Decision Date1979-06-27
Product CodeFQZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TEMPO2-I DISPOSABLE THERMOMETERS is the device name listed in this FDA 510(k) record. The listed applicant is Airlife, Inc.. It received FDA 510(k) clearance on 1979-06-27 under 510(k) number K790890. The device is classified under product code FQZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMPO2-I DISPOSABLE THERMOMETERS?

TEMPO2-I DISPOSABLE THERMOMETERS is a medical device that received FDA 510(k) clearance on 1979-06-27. The listed applicant is Airlife, Inc.. The 510(k) number is K790890.

When did TEMPO2-I DISPOSABLE THERMOMETERS receive FDA 510(k) clearance?

TEMPO2-I DISPOSABLE THERMOMETERS received FDA 510(k) clearance on 1979-06-27, under 510(k) number K790890.

Who is the listed applicant for TEMPO2-I DISPOSABLE THERMOMETERS?

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

What is the FDA product code for TEMPO2-I DISPOSABLE THERMOMETERS?

The FDA product code for TEMPO2-I DISPOSABLE THERMOMETERS is FQZ.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Airlife, Inc. 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.

K834573AQUA TRAPK834570VOLUME VENTILATOR CIRCUIT W/WATER TRAPK834077SINGLE USE NEBULIZER-ADJUST-AIR ENTRAINK833196VOLUME VENTILATOR CIRCUIT-NEBULIZERK833197TRACH SWIVE/CONNECTORK832725DUAL DIAL VENTURI STYLE MASK

View all 76 devices →

Related Devices (Code: FQZ)

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.

K110305CRY-ACTRACKERCAMBrymill Cryogenic CystemsK963049STERI-AID KITSteri-Aid, Inc.K946046DEROYAL TECHNOLOGICES, INC. LIQUID CRYSTAL SKIN TEMPERATURE STRIPDeroyal Critical Care, Div. Deroyal TechnologiesK894893POINT CHECKER COLOR STRIP THERMOMETERKyowa Medex Co., Ltd.K884612FRANKLIN COLLECTOR(R)Franklin Diagnostics, Inc.K881286TEMPA-DOT CLINICAL THERMOMETER SHEATHPymah Corp.

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.

↑