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FDA 510(k)

LIBERTY 9000 8-CH BREAST COIL WITH DISPOSABLE BIOPSY PLATE

K-Number: K041695 · 2004-07-23

ApplicantUsa Instruments, Inc.
Decision Date2004-07-23
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LIBERTY 9000 8-CH BREAST COIL WITH DISPOSABLE BIOPSY PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Usa Instruments, Inc.. It received FDA 510(k) clearance on 2004-07-23 under 510(k) number K041695. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIBERTY 9000 8-CH BREAST COIL WITH DISPOSABLE BIOPSY PLATE?

LIBERTY 9000 8-CH BREAST COIL WITH DISPOSABLE BIOPSY PLATE is a medical device that received FDA 510(k) clearance on 2004-07-23. The listed applicant is Usa Instruments, Inc.. The 510(k) number is K041695.

When did LIBERTY 9000 8-CH BREAST COIL WITH DISPOSABLE BIOPSY PLATE receive FDA 510(k) clearance?

LIBERTY 9000 8-CH BREAST COIL WITH DISPOSABLE BIOPSY PLATE received FDA 510(k) clearance on 2004-07-23, under 510(k) number K041695.

Who is the listed applicant for LIBERTY 9000 8-CH BREAST COIL WITH DISPOSABLE BIOPSY PLATE?

The FDA 510(k) record lists Usa Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIBERTY 9000 8-CH BREAST COIL WITH DISPOSABLE BIOPSY PLATE?

The FDA product code for LIBERTY 9000 8-CH BREAST COIL WITH DISPOSABLE BIOPSY PLATE is LNH.

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Other records listing Usa Instruments, Inc. as applicant

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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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