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FDA 510(k)

BO POWER SUPPLY

K-Number: K921046 · 1992-05-28

ApplicantResonex, Inc.
Decision Date1992-05-28
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BO POWER SUPPLY is the device name listed in this FDA 510(k) record. The listed applicant is Resonex, Inc.. It received FDA 510(k) clearance on 1992-05-28 under 510(k) number K921046. 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 BO POWER SUPPLY?

BO POWER SUPPLY is a medical device that received FDA 510(k) clearance on 1992-05-28. The listed applicant is Resonex, Inc.. The 510(k) number is K921046.

When did BO POWER SUPPLY receive FDA 510(k) clearance?

BO POWER SUPPLY received FDA 510(k) clearance on 1992-05-28, under 510(k) number K921046.

Who is the listed applicant for BO POWER SUPPLY?

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

What is the FDA product code for BO POWER SUPPLY?

The FDA product code for BO POWER SUPPLY is LNH.

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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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