FDA 510(k)

CHX=CHX PLUS

K-Number: K112250 · 2011-10-28

Decision Date2011-10-28

Product CodeKJJ

DecisionSubstantially Equivalent

Device Summary

CHX=CHX PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Inter-Med, Inc.. It received FDA 510(k) clearance on 2011-10-28 under 510(k) number K112250. The device is classified under product code KJJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHX=CHX PLUS?

CHX=CHX PLUS is a medical device that received FDA 510(k) clearance on 2011-10-28. The listed applicant is Inter-Med, Inc.. The 510(k) number is K112250.

When did CHX=CHX PLUS receive FDA 510(k) clearance?

CHX=CHX PLUS received FDA 510(k) clearance on 2011-10-28, under 510(k) number K112250.

Who is the listed applicant for CHX=CHX PLUS?

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

What is the FDA product code for CHX=CHX PLUS?

The FDA product code for CHX=CHX PLUS is KJJ.

Other records listing Inter-Med, Inc. as applicant

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Related Devices (Code: KJJ)

K250279RC-SwiftPrepBelport Company, Inc., Gingi-Pak K241354Sealer SolventInter-Med, Inc.K201785EPIEN Dental CleanserEpien Medical, Inc.K211813TritonInter-Med / Vista Dental K193357V-MixInter-Med/Vista Dental Products K193409Vista Rinse, Vista Rinse PlusInter-Med/Vista Dental Products

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.