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FDA 510(k)

ULTIMA WHEELCHAIR CUSHION

K-Number: K890653 · 1989-02-28

ApplicantClark Pillow Co., Inc.
Decision Date1989-02-28
Product CodeIMP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ULTIMA WHEELCHAIR CUSHION is the device name listed in this FDA 510(k) record. The listed applicant is Clark Pillow Co., Inc.. It received FDA 510(k) clearance on 1989-02-28 under 510(k) number K890653. The device is classified under product code IMP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTIMA WHEELCHAIR CUSHION?

ULTIMA WHEELCHAIR CUSHION is a medical device that received FDA 510(k) clearance on 1989-02-28. The listed applicant is Clark Pillow Co., Inc.. The 510(k) number is K890653.

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

ULTIMA WHEELCHAIR CUSHION received FDA 510(k) clearance on 1989-02-28, under 510(k) number K890653.

Who is the listed applicant for ULTIMA WHEELCHAIR CUSHION?

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

What is the FDA product code for ULTIMA WHEELCHAIR CUSHION?

The FDA product code for ULTIMA WHEELCHAIR CUSHION is IMP.

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.

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Related Devices (Code: IMP)

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

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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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