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FDA 510(k)

CARONY

K-Number: K002205 · 2000-08-10

ApplicantBruno Independent Living Aids, Inc.
Decision Date2000-08-10
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CARONY 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 2000-08-10 under 510(k) number K002205. 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 CARONY?

CARONY is a medical device that received FDA 510(k) clearance on 2000-08-10. The listed applicant is Bruno Independent Living Aids, Inc.. The 510(k) number is K002205.

When did CARONY receive FDA 510(k) clearance?

CARONY received FDA 510(k) clearance on 2000-08-10, under 510(k) number K002205.

Who is the listed applicant for CARONY?

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 CARONY?

The FDA product code for CARONY is IOR.

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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.

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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.

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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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