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)

DMI 250 SERIES POWER SURGERY TABLE

K-Number: K894789 · 1989-08-29

ApplicantM.D. Intl., Inc.
Decision Date1989-08-29
Product CodeJEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DMI 250 SERIES POWER SURGERY TABLE is the device name listed in this FDA 510(k) record. The listed applicant is M.D. Intl., Inc.. It received FDA 510(k) clearance on 1989-08-29 under 510(k) number K894789. The device is classified under product code JEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DMI 250 SERIES POWER SURGERY TABLE?

DMI 250 SERIES POWER SURGERY TABLE is a medical device that received FDA 510(k) clearance on 1989-08-29. The listed applicant is M.D. Intl., Inc.. The 510(k) number is K894789.

When did DMI 250 SERIES POWER SURGERY TABLE receive FDA 510(k) clearance?

DMI 250 SERIES POWER SURGERY TABLE received FDA 510(k) clearance on 1989-08-29, under 510(k) number K894789.

Who is the listed applicant for DMI 250 SERIES POWER SURGERY TABLE?

The FDA 510(k) record lists M.D. Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DMI 250 SERIES POWER SURGERY TABLE?

The FDA product code for DMI 250 SERIES POWER SURGERY TABLE is JEA.

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 M.D. Intl., Inc. 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.

K894788DMI SERIES 90 EXAMINATION TABLEK870832OXY-THERMK771249JOY LIGHT

Related Devices (Code: JEA)

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.

K953071STRYKER COMMAND2 OFFICE CONSOLEStryker InstrumentsK924094MEND APCMend Technologies, Inc.K910736JACKSON MULTIPURPOSE OPERATING TABLEOrthopedic Systems, Inc.K911522ARTHROBOT(TM) WRIST HOLDER ACCESSORYAndronic Devices, Ltd.K900290SKYTRON MODEL 1100 AND MODEL 142Skytron, Div. the Kmw Group, Inc.K881060OSI RIZZOLI TRAUMA TABLE (ELECTRIC VERSION)Orthopedic Systems, Inc.

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.

↑