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FDA 510(k)

MIGHTY AIR

K-Number: K974319 · 1998-01-22

ApplicantWheelchairs of Kansas
Decision Date1998-01-22
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MIGHTY AIR is the device name listed in this FDA 510(k) record. The listed applicant is Wheelchairs of Kansas. It received FDA 510(k) clearance on 1998-01-22 under 510(k) number K974319. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIGHTY AIR?

MIGHTY AIR is a medical device that received FDA 510(k) clearance on 1998-01-22. The listed applicant is Wheelchairs of Kansas. The 510(k) number is K974319.

When did MIGHTY AIR receive FDA 510(k) clearance?

MIGHTY AIR received FDA 510(k) clearance on 1998-01-22, under 510(k) number K974319.

Who is the listed applicant for MIGHTY AIR?

The FDA 510(k) record lists Wheelchairs of Kansas as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIGHTY AIR?

The FDA product code for MIGHTY AIR is FNM.

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 Wheelchairs of Kansas 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.

K970743BCW POWER ADVANTAGE WHEELCHAIRK961514BCW ADVANTAGE WHEELCHAIRK945047BCW 600 POWER WHEELCHAIR

Related Devices (Code: FNM)

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.

K973169PRESSURE GUARD SITE SELECT (A)Span-America Medical Systems, Inc.K972022ZAK-2000Cardio Systems, Inc.K974070PHYSIO/1000Physio Designs, Inc.K972549SIMPULSEKinetic Concepts, Inc.K970081SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEMCathay Consolidated, Inc.K955243BARIAIRKinetic Concepts, 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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