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FDA 510(k)

PEGASUS PROACTIVE WHEELCHAIR CUSHION

K-Number: K930742 · 1994-03-31

ApplicantPegasus Airwave, Inc.
Decision Date1994-03-31
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

PEGASUS PROACTIVE WHEELCHAIR CUSHION is the device name listed in this FDA 510(k) record. The listed applicant is Pegasus Airwave, Inc.. It received FDA 510(k) clearance on 1994-03-31 under 510(k) number K930742. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the PEGASUS PROACTIVE WHEELCHAIR CUSHION?

PEGASUS PROACTIVE WHEELCHAIR CUSHION is a medical device that received FDA 510(k) clearance on 1994-03-31. The listed applicant is Pegasus Airwave, Inc.. The 510(k) number is K930742.

When did PEGASUS PROACTIVE WHEELCHAIR CUSHION receive FDA 510(k) clearance?

PEGASUS PROACTIVE WHEELCHAIR CUSHION received FDA 510(k) clearance on 1994-03-31, under 510(k) number K930742.

Who is the listed applicant for PEGASUS PROACTIVE WHEELCHAIR CUSHION?

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

What is the FDA product code for PEGASUS PROACTIVE WHEELCHAIR CUSHION?

The FDA product code for PEGASUS PROACTIVE WHEELCHAIR CUSHION is ITI.

Related Clinical Trials

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Other records listing Pegasus Airwave, 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.

K944310PEGASUS BIWAVE PLUS SYSTEMK933004PEGASUS BIWAVE SYSTEMK874877PEGASUS AIRWAVE SYST/SPEC MATTRESS DECUBITUS ULCER

Related Devices (Code: ITI)

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.

K262582Electric wheelchair (GP100)Suzhou Green Pine Medical Co., Ltd.K262054Electric WheelchairYongkang Joymax Medical Technology Co., Ltd.K260053Power Wheelchair (OS-R-M01I)Beijing OrionStar Technology Co., Ltd.K260229Electric wheelchair (HC819N, HC830N, HC831N)Yongkang Hengyi Vehicle Co., Ltd.K261354Electric wheelchair (D03)Foshan Sowell Medical Technology Co., Ltd.K261149Electric Wheelchair (DY611A-2, DY612A-1)Zhejiang Lumbre Electric Appliance Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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