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FDA 510(k)

MEDLINE EXCEL WHEELCHAIRS

K-Number: K990463 · 1999-03-15

ApplicantMedline
Decision Date1999-03-15
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDLINE EXCEL WHEELCHAIRS is the device name listed in this FDA 510(k) record. The listed applicant is Medline. It received FDA 510(k) clearance on 1999-03-15 under 510(k) number K990463. 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 MEDLINE EXCEL WHEELCHAIRS?

MEDLINE EXCEL WHEELCHAIRS is a medical device that received FDA 510(k) clearance on 1999-03-15. The listed applicant is Medline. The 510(k) number is K990463.

When did MEDLINE EXCEL WHEELCHAIRS receive FDA 510(k) clearance?

MEDLINE EXCEL WHEELCHAIRS received FDA 510(k) clearance on 1999-03-15, under 510(k) number K990463.

Who is the listed applicant for MEDLINE EXCEL WHEELCHAIRS?

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

What is the FDA product code for MEDLINE EXCEL WHEELCHAIRS?

The FDA product code for MEDLINE EXCEL WHEELCHAIRS 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 Medline 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 11 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

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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