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FDA 510(k)

RELIANT

K-Number: K932397 · 1994-03-07

ApplicantAllan Walling Medical Equipment Co.
Decision Date1994-03-07
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RELIANT is the device name listed in this FDA 510(k) record. The listed applicant is Allan Walling Medical Equipment Co.. It received FDA 510(k) clearance on 1994-03-07 under 510(k) number K932397. 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 RELIANT?

RELIANT is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Allan Walling Medical Equipment Co.. The 510(k) number is K932397.

When did RELIANT receive FDA 510(k) clearance?

RELIANT received FDA 510(k) clearance on 1994-03-07, under 510(k) number K932397.

Who is the listed applicant for RELIANT?

The FDA 510(k) record lists Allan Walling Medical Equipment Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RELIANT?

The FDA product code for RELIANT is LKY.

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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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