FDA 510(k)

LOTUS PULMONARY FUNCTION FILTER, MODELS CPF 101, CPF 102, CPF 103

K-Number: K033518 · 2004-03-10

Decision Date2004-03-10

Product CodeBZG

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

LOTUS PULMONARY FUNCTION FILTER, MODELS CPF 101, CPF 102, CPF 103 is the device name listed in this FDA 510(k) record. The listed applicant is Custom Plastic Products. It received FDA 510(k) clearance on 2004-03-10 under 510(k) number K033518. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOTUS PULMONARY FUNCTION FILTER, MODELS CPF 101, CPF 102, CPF 103?

LOTUS PULMONARY FUNCTION FILTER, MODELS CPF 101, CPF 102, CPF 103 is a medical device that received FDA 510(k) clearance on 2004-03-10. The listed applicant is Custom Plastic Products. The 510(k) number is K033518.

When did LOTUS PULMONARY FUNCTION FILTER, MODELS CPF 101, CPF 102, CPF 103 receive FDA 510(k) clearance?

LOTUS PULMONARY FUNCTION FILTER, MODELS CPF 101, CPF 102, CPF 103 received FDA 510(k) clearance on 2004-03-10, under 510(k) number K033518.

Who is the listed applicant for LOTUS PULMONARY FUNCTION FILTER, MODELS CPF 101, CPF 102, CPF 103?

The FDA 510(k) record lists Custom Plastic Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOTUS PULMONARY FUNCTION FILTER, MODELS CPF 101, CPF 102, CPF 103?

The FDA product code for LOTUS PULMONARY FUNCTION FILTER, MODELS CPF 101, CPF 102, CPF 103 is BZG.

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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.