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FDA 510(k)

MERITS WHEELCHAIR

K-Number: K933662 · 1994-03-30

Decision Date1994-03-30
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

MERITS WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Merits Health Products., Inc.. It received FDA 510(k) clearance on 1994-03-30 under 510(k) number K933662. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the MERITS WHEELCHAIR?

MERITS WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1994-03-30. The listed applicant is Merits Health Products., Inc.. The 510(k) number is K933662.

When did MERITS WHEELCHAIR receive FDA 510(k) clearance?

MERITS WHEELCHAIR received FDA 510(k) clearance on 1994-03-30, under 510(k) number K933662.

Who is the listed applicant for MERITS WHEELCHAIR?

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

What is the FDA product code for MERITS WHEELCHAIR?

The FDA product code for MERITS WHEELCHAIR is ITI.

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 Merits Health Products., 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 12 devices →

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.

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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