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FDA 510(k)

THE PRECISIONIST

K-Number: K900493 · 1990-08-28

ApplicantParadigm Medical, Inc.
Decision Date1990-08-28
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THE PRECISIONIST 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 1990-08-28 under 510(k) number K900493. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE PRECISIONIST?

THE PRECISIONIST is a medical device that received FDA 510(k) clearance on 1990-08-28. The listed applicant is Paradigm Medical, Inc.. The 510(k) number is K900493.

When did THE PRECISIONIST receive FDA 510(k) clearance?

THE PRECISIONIST received FDA 510(k) clearance on 1990-08-28, under 510(k) number K900493.

Who is the listed applicant for THE PRECISIONIST?

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 THE PRECISIONIST?

The FDA product code for THE PRECISIONIST is HQC.

Related Clinical Trials

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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.

K960725MARPP PRESSURE MONITORING SYSTEM

Related Devices (Code: HQC)

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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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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