PROTEGE WHEELCHAIR
K-Number: K000602 · 2000-03-03
Advertisement
Device Summary
Frequently Asked Questions
What is the PROTEGE WHEELCHAIR?
PROTEGE WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2000-03-03. The listed applicant is Otto Bock Orthopedic Industry, Inc.. The 510(k) number is K000602.
When did PROTEGE WHEELCHAIR receive FDA 510(k) clearance?
PROTEGE WHEELCHAIR received FDA 510(k) clearance on 2000-03-03, under 510(k) number K000602.
Who is the listed applicant for PROTEGE WHEELCHAIR?
The FDA 510(k) record lists Otto Bock Orthopedic Industry, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROTEGE WHEELCHAIR?
The FDA product code for PROTEGE 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 Otto Bock Orthopedic Industry, 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: 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.
Advertisement