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)

MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE

K-Number: K915393 · 1991-12-17

ApplicantMdt Corp., Inc.
Decision Date1991-12-17
Product CodeGDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Mdt Corp., Inc.. It received FDA 510(k) clearance on 1991-12-17 under 510(k) number K915393. The device is classified under product code GDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE?

MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE is a medical device that received FDA 510(k) clearance on 1991-12-17. The listed applicant is Mdt Corp., Inc.. The 510(k) number is K915393.

When did MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE receive FDA 510(k) clearance?

MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE received FDA 510(k) clearance on 1991-12-17, under 510(k) number K915393.

Who is the listed applicant for MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE?

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

What is the FDA product code for MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE?

The FDA product code for MDT/SHAMPAINE MODEL 4900E SURGICAL TABLE is GDC.

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 Mdt Corp., 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.

K960777MDT UNISPORE AND SPOR-TEST BIOLOGICALINDICATORK942485MDT UROLOGY TABLEK942486IMAGE FULL POWER EXAMINATION/MINOR SURGERY TABLEK924380MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVEK926081DENTAL LIGHTK924955MDT/HARVEY MC-8 AND MC-10

View all 22 devices →

Related Devices (Code: GDC)

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.

K971390QUANTUM 3080SP SURGICAL TABLESTERIS CorporationK970807MOBILE OPERATING TABLE 1132.01Stierlen-Maquet AGK964273DURA-BOARD ARMBOARDAllen Medical Systems, Inc.K940616SKYTRON ELITE 3500 TABLESkytron, Div. the Kmw Group, Inc.K934744MIDMARK MAGNUM GENERAL SURGICAL TABLEMidmark Corp.K914758MDT/SHAMPAINE MODEL 4900B SURGICAL TABLEMdt Corp., 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.

↑