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FDA 510(k)

CROW MODEL 106A WHEELCHAIR

K-Number: K870294 · 1987-02-10

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

Device Summary

CROW MODEL 106A 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 K870294. 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 CROW MODEL 106A WHEELCHAIR?

CROW MODEL 106A 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 K870294.

When did CROW MODEL 106A WHEELCHAIR receive FDA 510(k) clearance?

CROW MODEL 106A WHEELCHAIR received FDA 510(k) clearance on 1987-02-10, under 510(k) number K870294.

Who is the listed applicant for CROW MODEL 106A 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 CROW MODEL 106A WHEELCHAIR?

The FDA product code for CROW MODEL 106A WHEELCHAIR is IOR.

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.

Other records listing Redman, 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.

View all 16 devices →

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.

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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