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)

THERMALGRAPHIC ANALYSER

K-Number: K894772 · 1989-10-03

ApplicantMedtech Instruments
Decision Date1989-10-03
Product CodeHCS
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

THERMALGRAPHIC ANALYSER is the device name listed in this FDA 510(k) record. The listed applicant is Medtech Instruments. It received FDA 510(k) clearance on 1989-10-03 under 510(k) number K894772. The device is classified under product code HCS. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMALGRAPHIC ANALYSER?

THERMALGRAPHIC ANALYSER is a medical device that received FDA 510(k) clearance on 1989-10-03. The listed applicant is Medtech Instruments. The 510(k) number is K894772.

When did THERMALGRAPHIC ANALYSER receive FDA 510(k) clearance?

THERMALGRAPHIC ANALYSER received FDA 510(k) clearance on 1989-10-03, under 510(k) number K894772.

Who is the listed applicant for THERMALGRAPHIC ANALYSER?

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

What is the FDA product code for THERMALGRAPHIC ANALYSER?

The FDA product code for THERMALGRAPHIC ANALYSER is HCS.

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 Medtech Instruments 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.

K973584MEDTRONIC INSTENT ESOPHACOIL ESOPHAGEAL STENT SYSTEM AND ESOPHACOIL EXTENSION SYSTEM

Related Devices (Code: HCS)

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.

K981805POS T-7000Pos Technologies, Inc.K974208TYTRON C-3000Titronics Research & Development Co.K950986NEUROREADERArtronicsK840487T-METERK.J. ElectronicsK831995TRENDO-SCOPEGabriel Ent.K822795GABRIEL DIGITRENDGabriel Ent.

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.

↑