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FDA 510(k)

10 ADJUSTABLE BELT COIL

K-Number: K910269 · 1991-04-08

ApplicantResonex, Inc.
Decision Date1991-04-08
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

10 ADJUSTABLE BELT COIL is the device name listed in this FDA 510(k) record. The listed applicant is Resonex, Inc.. It received FDA 510(k) clearance on 1991-04-08 under 510(k) number K910269. 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 10 ADJUSTABLE BELT COIL?

10 ADJUSTABLE BELT COIL is a medical device that received FDA 510(k) clearance on 1991-04-08. The listed applicant is Resonex, Inc.. The 510(k) number is K910269.

When did 10 ADJUSTABLE BELT COIL receive FDA 510(k) clearance?

10 ADJUSTABLE BELT COIL received FDA 510(k) clearance on 1991-04-08, under 510(k) number K910269.

Who is the listed applicant for 10 ADJUSTABLE BELT COIL?

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 10 ADJUSTABLE BELT COIL?

The FDA product code for 10 ADJUSTABLE BELT COIL 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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