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FDA 510(k)

MARPP PRESSURE MONITORING SYSTEM

K-Number: K960725 · 1996-07-15

ApplicantParadigm Medical, Inc.
Decision Date1996-07-15
Product CodeKYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MARPP PRESSURE MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Paradigm Medical, Inc.. It received FDA 510(k) clearance on 1996-07-15 under 510(k) number K960725. The device is classified under product code KYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARPP PRESSURE MONITORING SYSTEM?

MARPP PRESSURE MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1996-07-15. The listed applicant is Paradigm Medical, Inc.. The 510(k) number is K960725.

When did MARPP PRESSURE MONITORING SYSTEM receive FDA 510(k) clearance?

MARPP PRESSURE MONITORING SYSTEM received FDA 510(k) clearance on 1996-07-15, under 510(k) number K960725.

Who is the listed applicant for MARPP PRESSURE MONITORING SYSTEM?

The FDA 510(k) record lists Paradigm Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARPP PRESSURE MONITORING SYSTEM?

The FDA product code for MARPP PRESSURE MONITORING SYSTEM is KYZ.

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.

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Other records listing Paradigm Medical, Inc. 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.

K900493THE PRECISIONIST

Related Devices (Code: KYZ)

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.

K201877OtoSet- Ear Cleaning SystemSafkan, Inc.K102563SINGLE CANNULA EXTENDED APPLICATORMicromedics, Inc.K092022TISSU TRANS HARVEST TUBINGShippert Medical Technologies Corp.K050797TISSU-TRANSShippert Medical Technologies Corp.K991254QS DELIVERY SYSTEMSub-Q, Inc.K982435IRRIGATION SYRINGE KITSub-Q, Inc.

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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