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)

POIRIER KID-ROLLER MANUAL WHEELCHAIR

K-Number: K874317 · 1987-11-17

ApplicantRoseburg SA
Decision Date1987-11-17
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

POIRIER KID-ROLLER MANUAL WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Roseburg SA. It received FDA 510(k) clearance on 1987-11-17 under 510(k) number K874317. 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 POIRIER KID-ROLLER MANUAL WHEELCHAIR?

POIRIER KID-ROLLER MANUAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1987-11-17. The listed applicant is Roseburg SA. The 510(k) number is K874317.

When did POIRIER KID-ROLLER MANUAL WHEELCHAIR receive FDA 510(k) clearance?

POIRIER KID-ROLLER MANUAL WHEELCHAIR received FDA 510(k) clearance on 1987-11-17, under 510(k) number K874317.

Who is the listed applicant for POIRIER KID-ROLLER MANUAL WHEELCHAIR?

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

What is the FDA product code for POIRIER KID-ROLLER MANUAL WHEELCHAIR?

The FDA product code for POIRIER KID-ROLLER MANUAL WHEELCHAIR 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 Roseburg SA 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 24 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.

↑