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FDA 510(k)

PRI A PUS

K-Number: K832756 · 1983-11-28

ApplicantTrans Texas Medical Devices Corp.
Decision Date1983-11-28
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PRI A PUS is the device name listed in this FDA 510(k) record. The listed applicant is Trans Texas Medical Devices Corp.. It received FDA 510(k) clearance on 1983-11-28 under 510(k) number K832756. The device is classified under product code LKY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRI A PUS?

PRI A PUS is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Trans Texas Medical Devices Corp.. The 510(k) number is K832756.

When did PRI A PUS receive FDA 510(k) clearance?

PRI A PUS received FDA 510(k) clearance on 1983-11-28, under 510(k) number K832756.

Who is the listed applicant for PRI A PUS?

The FDA 510(k) record lists Trans Texas Medical Devices Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRI A PUS?

The FDA product code for PRI A PUS is LKY.

Related Devices (Code: LKY)

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.

K041573NANMA VACUUM PUMP PROXZEK MODEL 2M9498SNanma Mfg Co., Ltd.K032776VACURECT VACUUM CONSTRICTION DEVICEVacurect Manufacturing (Pty) , Ltd.K030119NANMA ADJUSTABLE CONSTRICTION RINGNanma Mfg Co., Ltd.K030913NANMA VACUUM PUMPNanma Mfg Co., Ltd.K013113MODIFICATION TO NANMA VACUUM PUMPNanma Mfg Co., Ltd.K013051NANMA ADJUSTABLE CONSTRICTION RINGNanma Mfg Co., Ltd.

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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