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FDA 510(k)

TENDERWET ACTIVE

K-Number: K040517 · 2004-03-25

ApplicantMedline Industries, Inc.
Decision Date2004-03-25
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

TENDERWET ACTIVE is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2004-03-25 under 510(k) number K040517. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TENDERWET ACTIVE?

TENDERWET ACTIVE is a medical device that received FDA 510(k) clearance on 2004-03-25. The listed applicant is Medline Industries, Inc.. The 510(k) number is K040517.

When did TENDERWET ACTIVE receive FDA 510(k) clearance?

TENDERWET ACTIVE received FDA 510(k) clearance on 2004-03-25, under 510(k) number K040517.

Who is the listed applicant for TENDERWET ACTIVE?

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

What is the FDA product code for TENDERWET ACTIVE?

The FDA product code for TENDERWET ACTIVE is MGQ.

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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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