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FDA 510(k)

PARI-MASTER MODIFICATION

K-Number: K935540 · 1995-03-17

Decision Date1995-03-17
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PARI-MASTER MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Pari Holding Co.. It received FDA 510(k) clearance on 1995-03-17 under 510(k) number K935540. 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 MODIFICATION?

PARI-MASTER MODIFICATION is a medical device that received FDA 510(k) clearance on 1995-03-17. The listed applicant is Pari Holding Co.. The 510(k) number is K935540.

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

PARI-MASTER MODIFICATION received FDA 510(k) clearance on 1995-03-17, under 510(k) number K935540.

Who is the listed applicant for PARI-MASTER MODIFICATION?

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

What is the FDA product code for PARI-MASTER MODIFICATION?

The FDA product code for PARI-MASTER MODIFICATION is CAF.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Pari Holding Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 8 devices →

Related Devices (Code: CAF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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