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FDA 510(k)

SIOUX MODEL 102ALW WHEELCHAIR

K-Number: K870295 · 1987-02-10

ApplicantRedman, Inc.
Decision Date1987-02-10
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SIOUX MODEL 102ALW WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Redman, Inc.. It received FDA 510(k) clearance on 1987-02-10 under 510(k) number K870295. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIOUX MODEL 102ALW WHEELCHAIR?

SIOUX MODEL 102ALW WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1987-02-10. The listed applicant is Redman, Inc.. The 510(k) number is K870295.

When did SIOUX MODEL 102ALW WHEELCHAIR receive FDA 510(k) clearance?

SIOUX MODEL 102ALW WHEELCHAIR received FDA 510(k) clearance on 1987-02-10, under 510(k) number K870295.

Who is the listed applicant for SIOUX MODEL 102ALW WHEELCHAIR?

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

What is the FDA product code for SIOUX MODEL 102ALW WHEELCHAIR?

The FDA product code for SIOUX MODEL 102ALW WHEELCHAIR is IOR.

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Other records listing Redman, Inc. as applicant

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Related Devices (Code: IOR)

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.

K253762ErgoSteel (ES0001/696)Strongback Mobility AG C/O Blueaudit GmbHK261919Multifunctional wheelchair (YJ-059)Zhenjiang Assure Medical Equipment Co., Ltd.K260141Bariatric Heavy Duty Wheelchair (YJ-010V, YJ-010C)Zhenjiang Assure Medical Equipment Co., Ltd.K260145YJ-K1K2 Wheelchair (YJ-013F)Zhenjiang Assure Medical Equipment Co., Ltd.K260144Reclining wheelchair (YJ-013L)Zhenjiang Assure Medical Equipment Co., Ltd.K261571Manual Wheelchair (H008, PCK7)Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.

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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