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FDA 510(k)

MODEL MPFT-01, GENESIS

K-Number: K934574 · 1994-03-04

ApplicantInternational Medical Designs, Inc.
Decision Date1994-03-04
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL MPFT-01, GENESIS is the device name listed in this FDA 510(k) record. The listed applicant is International Medical Designs, Inc.. It received FDA 510(k) clearance on 1994-03-04 under 510(k) number K934574. The device is classified under product code IXR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL MPFT-01, GENESIS?

MODEL MPFT-01, GENESIS is a medical device that received FDA 510(k) clearance on 1994-03-04. The listed applicant is International Medical Designs, Inc.. The 510(k) number is K934574.

When did MODEL MPFT-01, GENESIS receive FDA 510(k) clearance?

MODEL MPFT-01, GENESIS received FDA 510(k) clearance on 1994-03-04, under 510(k) number K934574.

Who is the listed applicant for MODEL MPFT-01, GENESIS?

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

What is the FDA product code for MODEL MPFT-01, GENESIS?

The FDA product code for MODEL MPFT-01, GENESIS is IXR.

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.

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Other records listing International Medical Designs, 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.

K942019MODEL FP-100

Related Devices (Code: IXR)

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.

K000412VISION R/F TILTING TABLEVilla Sistemi Medicali S.P.A.K973039LEGACY/LEGACY-D TABLEGE Medical SystemsK971128CAP-35B III/CINE 275Jamieson Film Co.K970640PHILIPS EASY DIAGNOSTPhilips Medical Systems North America, Inc.K965105ELECTROPHYSIOLOGY TILT TABLE MODEL #9660U.S. Imaging Tables, Inc.K965096FLUOROVIEW SERIES FLUOROSCOPIC TABLESU.S. Imaging Tables, 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.

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