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FDA 510(k)

MOIST PUNCTAL PLUG SYSTEM

K-Number: K021936 · 2002-10-16

ApplicantMoist Medical, Inc.
Decision Date2002-10-16
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

MOIST PUNCTAL PLUG SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Moist Medical, Inc.. It received FDA 510(k) clearance on 2002-10-16 under 510(k) number K021936. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOIST PUNCTAL PLUG SYSTEM?

MOIST PUNCTAL PLUG SYSTEM is a medical device that received FDA 510(k) clearance on 2002-10-16. The listed applicant is Moist Medical, Inc.. The 510(k) number is K021936.

When did MOIST PUNCTAL PLUG SYSTEM receive FDA 510(k) clearance?

MOIST PUNCTAL PLUG SYSTEM received FDA 510(k) clearance on 2002-10-16, under 510(k) number K021936.

Who is the listed applicant for MOIST PUNCTAL PLUG SYSTEM?

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

What is the FDA product code for MOIST PUNCTAL PLUG SYSTEM?

The FDA product code for MOIST PUNCTAL PLUG SYSTEM is LZU.

Related Clinical Trials

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Related Devices (Code: LZU)

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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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