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)

HOVERTRANS TRANSFORMER WITH POWER DRIVE MODEL HTT-650P

K-Number: K102236 · 2010-11-18

ApplicantD.T. Davis Enterprises Ltd. T/A Hovertech Int'L
Decision Date2010-11-18
Product CodeINK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HOVERTRANS TRANSFORMER WITH POWER DRIVE MODEL HTT-650P is the device name listed in this FDA 510(k) record. The listed applicant is D.T. Davis Enterprises Ltd. T/A Hovertech Int'L. It received FDA 510(k) clearance on 2010-11-18 under 510(k) number K102236. The device is classified under product code INK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOVERTRANS TRANSFORMER WITH POWER DRIVE MODEL HTT-650P?

HOVERTRANS TRANSFORMER WITH POWER DRIVE MODEL HTT-650P is a medical device that received FDA 510(k) clearance on 2010-11-18. The listed applicant is D.T. Davis Enterprises Ltd. T/A Hovertech Int'L. The 510(k) number is K102236.

When did HOVERTRANS TRANSFORMER WITH POWER DRIVE MODEL HTT-650P receive FDA 510(k) clearance?

HOVERTRANS TRANSFORMER WITH POWER DRIVE MODEL HTT-650P received FDA 510(k) clearance on 2010-11-18, under 510(k) number K102236.

Who is the listed applicant for HOVERTRANS TRANSFORMER WITH POWER DRIVE MODEL HTT-650P?

The FDA 510(k) record lists D.T. Davis Enterprises Ltd. T/A Hovertech Int'L as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOVERTRANS TRANSFORMER WITH POWER DRIVE MODEL HTT-650P?

The FDA product code for HOVERTRANS TRANSFORMER WITH POWER DRIVE MODEL HTT-650P is INK.

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 D.T. Davis Enterprises Ltd. T/A Hovertech Int'L 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.

K121287HT-WEDGE

Related Devices (Code: INK)

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.

K152056Winco Model S550 StretchairWinco Manufacturing, LLCK112502PROCEDURAL STRECHER WITH INTELLIDRIVE P8000Hill-Rom Co.K110671WINCO STRETCHAIRWinco Mfg., LLCK091043POWER DRIVE CHAIR, MODEL: TMM6Transmotion Medical, Inc.K051861THE SAVION INDUSTRIES MEDI-CRUISER MODEL MS777Savion Industries, Ltd.K041924HAUSTED POWERTRAN SERIES STRETCHERSTERIS Corporation

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.

↑