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FDA 510(k)

NANMA VACUUM PUMP PROXZEK MODEL 2M9498S

K-Number: K041573 · 2004-08-25

Decision Date2004-08-25
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NANMA VACUUM PUMP PROXZEK MODEL 2M9498S is the device name listed in this FDA 510(k) record. The listed applicant is Nanma Mfg Co., Ltd.. It received FDA 510(k) clearance on 2004-08-25 under 510(k) number K041573. 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 NANMA VACUUM PUMP PROXZEK MODEL 2M9498S?

NANMA VACUUM PUMP PROXZEK MODEL 2M9498S is a medical device that received FDA 510(k) clearance on 2004-08-25. The listed applicant is Nanma Mfg Co., Ltd.. The 510(k) number is K041573.

When did NANMA VACUUM PUMP PROXZEK MODEL 2M9498S receive FDA 510(k) clearance?

NANMA VACUUM PUMP PROXZEK MODEL 2M9498S received FDA 510(k) clearance on 2004-08-25, under 510(k) number K041573.

Who is the listed applicant for NANMA VACUUM PUMP PROXZEK MODEL 2M9498S?

The FDA 510(k) record lists Nanma Mfg Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NANMA VACUUM PUMP PROXZEK MODEL 2M9498S?

The FDA product code for NANMA VACUUM PUMP PROXZEK MODEL 2M9498S is LKY.

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 Nanma Mfg Co., Ltd. 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.

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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.

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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