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FDA 510(k)

BEAMMED SUNLIGHT MINIOMNI BONE SONOMETER

K-Number: K110646 · 2011-10-12

ApplicantBeam-Med, Ltd.
Decision Date2011-10-12
Product CodeMUA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BEAMMED SUNLIGHT MINIOMNI BONE SONOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Beam-Med, Ltd.. It received FDA 510(k) clearance on 2011-10-12 under 510(k) number K110646. The device is classified under product code MUA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEAMMED SUNLIGHT MINIOMNI BONE SONOMETER?

BEAMMED SUNLIGHT MINIOMNI BONE SONOMETER is a medical device that received FDA 510(k) clearance on 2011-10-12. The listed applicant is Beam-Med, Ltd.. The 510(k) number is K110646.

When did BEAMMED SUNLIGHT MINIOMNI BONE SONOMETER receive FDA 510(k) clearance?

BEAMMED SUNLIGHT MINIOMNI BONE SONOMETER received FDA 510(k) clearance on 2011-10-12, under 510(k) number K110646.

Who is the listed applicant for BEAMMED SUNLIGHT MINIOMNI BONE SONOMETER?

The FDA 510(k) record lists Beam-Med, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BEAMMED SUNLIGHT MINIOMNI BONE SONOMETER?

The FDA product code for BEAMMED SUNLIGHT MINIOMNI BONE SONOMETER is MUA.

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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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