BRUNO ELAN STAIRWAY ELEVATOR
K-Number: K113308 · 2012-02-01
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Device Summary
Frequently Asked Questions
What is the BRUNO ELAN STAIRWAY ELEVATOR?
BRUNO ELAN STAIRWAY ELEVATOR is a medical device that received FDA 510(k) clearance on 2012-02-01. The listed applicant is Bruno Independent Living Aids, Inc.. The 510(k) number is K113308.
When did BRUNO ELAN STAIRWAY ELEVATOR receive FDA 510(k) clearance?
BRUNO ELAN STAIRWAY ELEVATOR received FDA 510(k) clearance on 2012-02-01, under 510(k) number K113308.
Who is the listed applicant for BRUNO ELAN STAIRWAY ELEVATOR?
The FDA 510(k) record lists Bruno Independent Living Aids, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BRUNO ELAN STAIRWAY ELEVATOR?
The FDA product code for BRUNO ELAN STAIRWAY ELEVATOR is ILK.
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 Bruno Independent Living Aids, 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: ILK)
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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