FDA 510(k)

CON-KIT

K-Number: K941129 · 1994-05-09

Decision Date1994-05-09

Product CodeLKS

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

CON-KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Chemical Corp.. It received FDA 510(k) clearance on 1994-05-09 under 510(k) number K941129. The device is classified under product code LKS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CON-KIT?

CON-KIT is a medical device that received FDA 510(k) clearance on 1994-05-09. The listed applicant is Medical Chemical Corp.. The 510(k) number is K941129.

When did CON-KIT receive FDA 510(k) clearance?

CON-KIT received FDA 510(k) clearance on 1994-05-09, under 510(k) number K941129.

Who is the listed applicant for CON-KIT?

The FDA 510(k) record lists Medical Chemical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CON-KIT?

The FDA product code for CON-KIT is LKS.

Related Devices (Code: LKS)

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.

K053257PARA-PRO FC50Alpha-Tec Systems, Inc.K021420PARACON II/FECAL CONCENTRATOR IIPara Scientific Co.K980077PARA-PAK SPINCONMeridian Diagnostics, Inc.K941110PARAKITHardy Diagnostics K933370STOOL TRANSPORT/PROCESSORSage Products, Inc.K935316PARASAFE(R) FIXATIVEScientific Device Laboratory, Inc.

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.