RANGEROLLER
K-Number: K915152 · 1992-01-09
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Device Summary
Frequently Asked Questions
What is the RANGEROLLER?
RANGEROLLER is a medical device that received FDA 510(k) clearance on 1992-01-09. The listed applicant is Excel Mobility Products, Inc.. The 510(k) number is K915152.
When did RANGEROLLER receive FDA 510(k) clearance?
RANGEROLLER received FDA 510(k) clearance on 1992-01-09, under 510(k) number K915152.
Who is the listed applicant for RANGEROLLER?
The FDA 510(k) record lists Excel Mobility Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RANGEROLLER?
The FDA product code for RANGEROLLER 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 Excel Mobility 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: 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
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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