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FDA 510(k)

SMART PLUG, MODEL 500; SMARTPLUG FORCEPS, MODEL 502; PUSH ROD, MODEL 503

K-Number: K022043 · 2002-10-18

ApplicantMedennium, Inc.
Decision Date2002-10-18
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

SMART PLUG, MODEL 500; SMARTPLUG FORCEPS, MODEL 502; PUSH ROD, MODEL 503 is the device name listed in this FDA 510(k) record. The listed applicant is Medennium, Inc.. It received FDA 510(k) clearance on 2002-10-18 under 510(k) number K022043. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMART PLUG, MODEL 500; SMARTPLUG FORCEPS, MODEL 502; PUSH ROD, MODEL 503?

SMART PLUG, MODEL 500; SMARTPLUG FORCEPS, MODEL 502; PUSH ROD, MODEL 503 is a medical device that received FDA 510(k) clearance on 2002-10-18. The listed applicant is Medennium, Inc.. The 510(k) number is K022043.

When did SMART PLUG, MODEL 500; SMARTPLUG FORCEPS, MODEL 502; PUSH ROD, MODEL 503 receive FDA 510(k) clearance?

SMART PLUG, MODEL 500; SMARTPLUG FORCEPS, MODEL 502; PUSH ROD, MODEL 503 received FDA 510(k) clearance on 2002-10-18, under 510(k) number K022043.

Who is the listed applicant for SMART PLUG, MODEL 500; SMARTPLUG FORCEPS, MODEL 502; PUSH ROD, MODEL 503?

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

What is the FDA product code for SMART PLUG, MODEL 500; SMARTPLUG FORCEPS, MODEL 502; PUSH ROD, MODEL 503?

The FDA product code for SMART PLUG, MODEL 500; SMARTPLUG FORCEPS, MODEL 502; PUSH ROD, MODEL 503 is LZU.

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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Related Devices (Code: LZU)

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

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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