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FDA 510(k)

BRUNO VERTICAL PLATFORM LIFT, MODEL VPL-3100

K-Number: K061514 · 2006-07-13

Decision Date2006-07-13
Product CodeING
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BRUNO VERTICAL PLATFORM LIFT, MODEL VPL-3100 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 2006-07-13 under 510(k) number K061514. The device is classified under product code ING. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRUNO VERTICAL PLATFORM LIFT, MODEL VPL-3100?

BRUNO VERTICAL PLATFORM LIFT, MODEL VPL-3100 is a medical device that received FDA 510(k) clearance on 2006-07-13. The listed applicant is Bruno Independent Living Aids, Inc.. The 510(k) number is K061514.

When did BRUNO VERTICAL PLATFORM LIFT, MODEL VPL-3100 receive FDA 510(k) clearance?

BRUNO VERTICAL PLATFORM LIFT, MODEL VPL-3100 received FDA 510(k) clearance on 2006-07-13, under 510(k) number K061514.

Who is the listed applicant for BRUNO VERTICAL PLATFORM LIFT, MODEL VPL-3100?

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 VERTICAL PLATFORM LIFT, MODEL VPL-3100?

The FDA product code for BRUNO VERTICAL PLATFORM LIFT, MODEL VPL-3100 is ING.

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.

View all 12 devices →

Related Devices (Code: ING)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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