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FDA 510(k)

DAKOTA MODEL 102C WHEELCHAIR

K-Number: K870297 · 1987-02-10

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

Device Summary

DAKOTA MODEL 102C 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 K870297. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAKOTA MODEL 102C WHEELCHAIR?

DAKOTA MODEL 102C 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 K870297.

When did DAKOTA MODEL 102C WHEELCHAIR receive FDA 510(k) clearance?

DAKOTA MODEL 102C WHEELCHAIR received FDA 510(k) clearance on 1987-02-10, under 510(k) number K870297.

Who is the listed applicant for DAKOTA MODEL 102C 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 DAKOTA MODEL 102C WHEELCHAIR?

The FDA product code for DAKOTA MODEL 102C WHEELCHAIR is ITI.

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Other records listing Redman, Inc. as applicant

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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.

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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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