FDA 510(k)

CIDEX ACTIVATED DIALDEHYDE SOLUTION

K-Number: K924434 · 1994-03-29

ApplicantJohnson & Johnson Medical, Inc.

Decision Date1994-03-29

Product CodeLRJ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

CIDEX ACTIVATED DIALDEHYDE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Medical, Inc.. It received FDA 510(k) clearance on 1994-03-29 under 510(k) number K924434. The device is classified under product code LRJ. It was reviewed by the HO advisory panel. Product code LRJ falls under the category of Clinical Lab, which includes general clinical laboratory instruments. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIDEX ACTIVATED DIALDEHYDE SOLUTION?

CIDEX ACTIVATED DIALDEHYDE SOLUTION is a medical device that received FDA 510(k) clearance on 1994-03-29. The listed applicant is Johnson & Johnson Medical, Inc.. The 510(k) number is K924434.

When did CIDEX ACTIVATED DIALDEHYDE SOLUTION receive FDA 510(k) clearance?

CIDEX ACTIVATED DIALDEHYDE SOLUTION received FDA 510(k) clearance on 1994-03-29, under 510(k) number K924434.

Who is the listed applicant for CIDEX ACTIVATED DIALDEHYDE SOLUTION?

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

What is the FDA product code for CIDEX ACTIVATED DIALDEHYDE SOLUTION?

The FDA product code for CIDEX ACTIVATED DIALDEHYDE SOLUTION is LRJ. This falls under the Clinical Lab category.

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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.