FDA 510(k)

BANICIDE LIQUID CHEMICAL STERILANT/HIGH-LEVEL DISINFECTANT

K-Number: K012889 · 2003-05-27

Decision Date2003-05-27

Product CodeMED

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

BANICIDE LIQUID CHEMICAL STERILANT/HIGH-LEVEL DISINFECTANT is the device name listed in this FDA 510(k) record. The listed applicant is Pascal Co., Inc.. It received FDA 510(k) clearance on 2003-05-27 under 510(k) number K012889. 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 BANICIDE LIQUID CHEMICAL STERILANT/HIGH-LEVEL DISINFECTANT?

BANICIDE LIQUID CHEMICAL STERILANT/HIGH-LEVEL DISINFECTANT is a medical device that received FDA 510(k) clearance on 2003-05-27. The listed applicant is Pascal Co., Inc.. The 510(k) number is K012889.

When did BANICIDE LIQUID CHEMICAL STERILANT/HIGH-LEVEL DISINFECTANT receive FDA 510(k) clearance?

BANICIDE LIQUID CHEMICAL STERILANT/HIGH-LEVEL DISINFECTANT received FDA 510(k) clearance on 2003-05-27, under 510(k) number K012889.

Who is the listed applicant for BANICIDE LIQUID CHEMICAL STERILANT/HIGH-LEVEL DISINFECTANT?

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

What is the FDA product code for BANICIDE LIQUID CHEMICAL STERILANT/HIGH-LEVEL DISINFECTANT?

The FDA product code for BANICIDE LIQUID CHEMICAL STERILANT/HIGH-LEVEL DISINFECTANT 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.