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FDA 510(k)

BRUNO ELECTRA-RIDE, MODEL SRE-2700

K-Number: K022509 · 2002-08-13

ApplicantBruno Independent Living Aids, Inc.
Decision Date2002-08-13
Product CodeILK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BRUNO ELECTRA-RIDE, MODEL SRE-2700 is the device name listed in this FDA 510(k) record. The listed applicant is Bruno Independent Living Aids, Inc.. It received FDA 510(k) clearance on 2002-08-13 under 510(k) number K022509. The device is classified under product code ILK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRUNO ELECTRA-RIDE, MODEL SRE-2700?

BRUNO ELECTRA-RIDE, MODEL SRE-2700 is a medical device that received FDA 510(k) clearance on 2002-08-13. The listed applicant is Bruno Independent Living Aids, Inc.. The 510(k) number is K022509.

When did BRUNO ELECTRA-RIDE, MODEL SRE-2700 receive FDA 510(k) clearance?

BRUNO ELECTRA-RIDE, MODEL SRE-2700 received FDA 510(k) clearance on 2002-08-13, under 510(k) number K022509.

Who is the listed applicant for BRUNO ELECTRA-RIDE, MODEL SRE-2700?

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 ELECTRA-RIDE, MODEL SRE-2700?

The FDA product code for BRUNO ELECTRA-RIDE, MODEL SRE-2700 is ILK.

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Other records listing Bruno Independent Living Aids, Inc. as applicant

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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.

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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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