PARI-MASTER MODIFICATION
K-Number: K935540 · 1995-03-17
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Device Summary
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.
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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