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FDA 510(k)

PARI FILTER/VALVE SET

K-Number: K926455 · 1993-09-28

ApplicantPaul Ritzau Pari-Werk GmbH
Decision Date1993-09-28
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PARI FILTER/VALVE SET is the device name listed in this FDA 510(k) record. The listed applicant is Paul Ritzau Pari-Werk GmbH. It received FDA 510(k) clearance on 1993-09-28 under 510(k) number K926455. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARI FILTER/VALVE SET?

PARI FILTER/VALVE SET is a medical device that received FDA 510(k) clearance on 1993-09-28. The listed applicant is Paul Ritzau Pari-Werk GmbH. The 510(k) number is K926455.

When did PARI FILTER/VALVE SET receive FDA 510(k) clearance?

PARI FILTER/VALVE SET received FDA 510(k) clearance on 1993-09-28, under 510(k) number K926455.

Who is the listed applicant for PARI FILTER/VALVE SET?

The FDA 510(k) record lists Paul Ritzau Pari-Werk GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PARI FILTER/VALVE SET?

The FDA product code for PARI FILTER/VALVE SET is CAF.

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Official Source

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