FDA 510(k)

CIDEX FORMULA 7* LONG-LIFE ACTIVATED DIALDEHYDE

K-Number: K924334 · 1994-03-29

ApplicantJohnson & Johnson Medical, Inc.

Decision Date1994-03-29

Product CodeMED

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

CIDEX FORMULA 7* LONG-LIFE ACTIVATED DIALDEHYDE 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 K924334. The device is classified under product code MED. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIDEX FORMULA 7* LONG-LIFE ACTIVATED DIALDEHYDE?

CIDEX FORMULA 7* LONG-LIFE ACTIVATED DIALDEHYDE 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 K924334.

When did CIDEX FORMULA 7* LONG-LIFE ACTIVATED DIALDEHYDE receive FDA 510(k) clearance?

CIDEX FORMULA 7* LONG-LIFE ACTIVATED DIALDEHYDE received FDA 510(k) clearance on 1994-03-29, under 510(k) number K924334.

Who is the listed applicant for CIDEX FORMULA 7* LONG-LIFE ACTIVATED DIALDEHYDE?

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 FORMULA 7* LONG-LIFE ACTIVATED DIALDEHYDE?

The FDA product code for CIDEX FORMULA 7* LONG-LIFE ACTIVATED DIALDEHYDE is MED.

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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.