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)

THERMOPLATE

K-Number: K991263 · 1999-07-08

ApplicantTokai Hit Co., Ltd.
Decision Date1999-07-08
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THERMOPLATE is the device name listed in this FDA 510(k) record. The listed applicant is Tokai Hit Co., Ltd.. It received FDA 510(k) clearance on 1999-07-08 under 510(k) number K991263. The device is classified under product code MQG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMOPLATE?

THERMOPLATE is a medical device that received FDA 510(k) clearance on 1999-07-08. The listed applicant is Tokai Hit Co., Ltd.. The 510(k) number is K991263.

When did THERMOPLATE receive FDA 510(k) clearance?

THERMOPLATE received FDA 510(k) clearance on 1999-07-08, under 510(k) number K991263.

Who is the listed applicant for THERMOPLATE?

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

What is the FDA product code for THERMOPLATE?

The FDA product code for THERMOPLATE is MQG.

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

Related Devices (Code: MQG)

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.

K261083Wallace® Aspiration Pump (WAPV1); Wallace® Pump Filter Connector (WFC); Wallace® Vacuum Connection Kit (WVCK)CooperSurgical, Inc.K260194Vacuum Pump (Model: AD-VPUM-500)Sheng Sheng Yi (Beijing) Technology Company LimitedK242684Harioculture TL-16 Time-lapse IncubatorHua Yue Medical Technology Co., Ltd.K232493Embryo Real-time Incubator (TLS301), Embryo Real-time Culture Dish (MC 2004)Wuhan Huchuang Union Technology Co., Ltd.K180188Geri Embryo Incubator with Geri Connect and Geri Assess Software, and Geri DishGenea Biomedx Pty, Ltd.K173264EmbryoScope+Vitrolife A/S

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.

↑