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FDA 510(k)

CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT

K-Number: K902625 · 1990-10-26

ApplicantLiaoning-Usa Corp.
Decision Date1990-10-26
Product CodeFLK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT is the device name listed in this FDA 510(k) record. The listed applicant is Liaoning-Usa Corp.. It received FDA 510(k) clearance on 1990-10-26 under 510(k) number K902625. The device is classified under product code FLK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT?

CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT is a medical device that received FDA 510(k) clearance on 1990-10-26. The listed applicant is Liaoning-Usa Corp.. The 510(k) number is K902625.

When did CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT receive FDA 510(k) clearance?

CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT received FDA 510(k) clearance on 1990-10-26, under 510(k) number K902625.

Who is the listed applicant for CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT?

The FDA 510(k) record lists Liaoning-Usa Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT?

The FDA product code for CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT is FLK.

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 Liaoning-Usa Corp. 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.

K911921DISPOSABLE ISOLATION GOWNK905487VARIOUS TYPES OF STETHOSCOPESK910623GAUZE SPONGES ABSORBENT GAUZE ROLLSK892781ANTELOPE BRAND PATIENT EXAMINATION GLOVESK892774PATIENT EXAMINATION GLOVES

Related Devices (Code: FLK)

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.

K960185AMSINO CLINICAL THERMOMETERAmsia Intl., Inc.K960224GERATHERM MERCUIRY FREE CLINICAL THERMOMETERRg Ent., Inc.K953465KENTEMPKentron Health Care, Inc.K942483CLINICAL GLASS THERMOMETERMakol Medical Instruments Corp.K941673MEDIAID UNIVERSAL THERMOMETERPolymedica Industries, Inc.K940380AMG MED BRAND CLINICAL GLASS THERMOMETERAmg Medical, Inc.

Official Source

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

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