Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

WHEELCHAIR MODEL STS

K-Number: K071390 · 2007-07-20

Decision Date2007-07-20
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHEELCHAIR MODEL STS is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Products, Inc.. It received FDA 510(k) clearance on 2007-07-20 under 510(k) number K071390. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHEELCHAIR MODEL STS?

WHEELCHAIR MODEL STS is a medical device that received FDA 510(k) clearance on 2007-07-20. The listed applicant is Innovative Products, Inc.. The 510(k) number is K071390.

When did WHEELCHAIR MODEL STS receive FDA 510(k) clearance?

WHEELCHAIR MODEL STS received FDA 510(k) clearance on 2007-07-20, under 510(k) number K071390.

Who is the listed applicant for WHEELCHAIR MODEL STS?

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

What is the FDA product code for WHEELCHAIR MODEL STS?

The FDA product code for WHEELCHAIR MODEL STS is IPL.

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 Innovative 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.

Related Devices (Code: IPL)

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.

↑