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FDA 510(k)

ACCESS BREAST COIL 4/SMS

K-Number: K060547 · 2006-03-29

Decision Date2006-03-29
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACCESS BREAST COIL 4/SMS is the device name listed in this FDA 510(k) record. The listed applicant is Confirma, Inc.. It received FDA 510(k) clearance on 2006-03-29 under 510(k) number K060547. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCESS BREAST COIL 4/SMS?

ACCESS BREAST COIL 4/SMS is a medical device that received FDA 510(k) clearance on 2006-03-29. The listed applicant is Confirma, Inc.. The 510(k) number is K060547.

When did ACCESS BREAST COIL 4/SMS receive FDA 510(k) clearance?

ACCESS BREAST COIL 4/SMS received FDA 510(k) clearance on 2006-03-29, under 510(k) number K060547.

Who is the listed applicant for ACCESS BREAST COIL 4/SMS?

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

What is the FDA product code for ACCESS BREAST COIL 4/SMS?

The FDA product code for ACCESS BREAST COIL 4/SMS is MOS.

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 Confirma, 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 9 devices →

Related Devices (Code: MOS)

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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