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FDA 510(k)

PARI-MASTER

K-Number: K912805 · 1992-01-15

ApplicantPaul Ritzau Pari GmbH
Decision Date1992-01-15
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PARI-MASTER is the device name listed in this FDA 510(k) record. The listed applicant is Paul Ritzau Pari GmbH. It received FDA 510(k) clearance on 1992-01-15 under 510(k) number K912805. 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-MASTER?

PARI-MASTER is a medical device that received FDA 510(k) clearance on 1992-01-15. The listed applicant is Paul Ritzau Pari GmbH. The 510(k) number is K912805.

When did PARI-MASTER receive FDA 510(k) clearance?

PARI-MASTER received FDA 510(k) clearance on 1992-01-15, under 510(k) number K912805.

Who is the listed applicant for PARI-MASTER?

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

What is the FDA product code for PARI-MASTER?

The FDA product code for PARI-MASTER is CAF.

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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.

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