FDA 510(k)

PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR

K-Number: K932922 · 1995-07-03

Decision Date1995-07-03

Product CodeMED

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cottrell, Ltd.. It received FDA 510(k) clearance on 1995-07-03 under 510(k) number K932922. 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 PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR?

PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR is a medical device that received FDA 510(k) clearance on 1995-07-03. The listed applicant is Cottrell, Ltd.. The 510(k) number is K932922.

When did PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR receive FDA 510(k) clearance?

PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR received FDA 510(k) clearance on 1995-07-03, under 510(k) number K932922.

Who is the listed applicant for PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR?

The FDA 510(k) record lists Cottrell, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR?

The FDA product code for PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR 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.