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)

TEMP/SC 200T -SKIN CONDUCTANCE/SKIN TEMP BIOFEEDBA

K-Number: K850642 · 1985-05-17

ApplicantThought Technology , Ltd.
Decision Date1985-05-17
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TEMP/SC 200T -SKIN CONDUCTANCE/SKIN TEMP BIOFEEDBA is the device name listed in this FDA 510(k) record. The listed applicant is Thought Technology , Ltd.. It received FDA 510(k) clearance on 1985-05-17 under 510(k) number K850642. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMP/SC 200T -SKIN CONDUCTANCE/SKIN TEMP BIOFEEDBA?

TEMP/SC 200T -SKIN CONDUCTANCE/SKIN TEMP BIOFEEDBA is a medical device that received FDA 510(k) clearance on 1985-05-17. The listed applicant is Thought Technology , Ltd.. The 510(k) number is K850642.

When did TEMP/SC 200T -SKIN CONDUCTANCE/SKIN TEMP BIOFEEDBA receive FDA 510(k) clearance?

TEMP/SC 200T -SKIN CONDUCTANCE/SKIN TEMP BIOFEEDBA received FDA 510(k) clearance on 1985-05-17, under 510(k) number K850642.

Who is the listed applicant for TEMP/SC 200T -SKIN CONDUCTANCE/SKIN TEMP BIOFEEDBA?

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

What is the FDA product code for TEMP/SC 200T -SKIN CONDUCTANCE/SKIN TEMP BIOFEEDBA?

The FDA product code for TEMP/SC 200T -SKIN CONDUCTANCE/SKIN TEMP BIOFEEDBA is HCC.

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 Thought Technology , 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.

K213197MyOnyx SystemK201014MyOnyx SystemK053434MYOTRAC INFINITI ELECTRICAL STIMULATORK053266MYOTRAC INFINITIK925681MYOTRAC2D/CSK935213INCONTROL

View all 22 devices →

Related Devices (Code: HCC)

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.

K233580A Breathing System (ABS)Deepwell Dtx, Inc.K222101PrismGraymatters Health , Ltd.K180173FreespiraPalo Alto Health Sciences, Inc.K163448GrindCare SystemSunstar Suisse S.A.K131586CANARY BREATHING SYSTEMPalo Alto Health Sciences, Inc.K122879EEGER4 MODEL 4.3Eeg Software, LLC

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.

↑