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FDA 510(k)

NON-MAGNETIC EXAMINATION TABLE FOR MAGNETIC RESONA

K-Number: K844578 · 1985-05-14

ApplicantEngineering Dynamics Corp.
Decision Date1985-05-14
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NON-MAGNETIC EXAMINATION TABLE FOR MAGNETIC RESONA is the device name listed in this FDA 510(k) record. The listed applicant is Engineering Dynamics Corp.. It received FDA 510(k) clearance on 1985-05-14 under 510(k) number K844578. The device is classified under product code FPO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-MAGNETIC EXAMINATION TABLE FOR MAGNETIC RESONA?

NON-MAGNETIC EXAMINATION TABLE FOR MAGNETIC RESONA is a medical device that received FDA 510(k) clearance on 1985-05-14. The listed applicant is Engineering Dynamics Corp.. The 510(k) number is K844578.

When did NON-MAGNETIC EXAMINATION TABLE FOR MAGNETIC RESONA receive FDA 510(k) clearance?

NON-MAGNETIC EXAMINATION TABLE FOR MAGNETIC RESONA received FDA 510(k) clearance on 1985-05-14, under 510(k) number K844578.

Who is the listed applicant for NON-MAGNETIC EXAMINATION TABLE FOR MAGNETIC RESONA?

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

What is the FDA product code for NON-MAGNETIC EXAMINATION TABLE FOR MAGNETIC RESONA?

The FDA product code for NON-MAGNETIC EXAMINATION TABLE FOR MAGNETIC RESONA is FPO.

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Other records listing Engineering Dynamics Corp. 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.

K871494UPPERCYCLE STATIONARY EXERCISE MACHINESK842108UNIVERSAL EXAMINATION TABLEK834098STATIONARY EXERCISE BICYCLEK828313DIGITAL RADIOGRAPHY EXAMINATION TABLEK802254GENERAL ULTRASOUND EXAM. TABLEK790545STRESS TESTING SYSTEM, LATERAL TILTING

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Related Devices (Code: FPO)

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K113598POWER-LOAD COT FASTENER SYSTEMStryker MedicalK072598IRSG I-MOVER FOR BEDSInternational Retail Services Group, LLCK972528DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)Dyna Corp.K955766ADULT-PEDIATRIC TRANSPORT SYSTEMInternational Biomedical, Inc.K962181HARE MODEL 2000 EZ LOADER MODEL 95555Dyna Corp.K961437WHEELED STRETCHERHill-Rom, 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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