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FDA 510(k)

MILTEX MEMBRANE TACK KIT

K-Number: K092855 · 2009-12-29

ApplicantMiltex, Inc.
Decision Date2009-12-29
Product CodeDZL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MILTEX MEMBRANE TACK KIT is the device name listed in this FDA 510(k) record. The listed applicant is Miltex, Inc.. It received FDA 510(k) clearance on 2009-12-29 under 510(k) number K092855. The device is classified under product code DZL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILTEX MEMBRANE TACK KIT?

MILTEX MEMBRANE TACK KIT is a medical device that received FDA 510(k) clearance on 2009-12-29. The listed applicant is Miltex, Inc.. The 510(k) number is K092855.

When did MILTEX MEMBRANE TACK KIT receive FDA 510(k) clearance?

MILTEX MEMBRANE TACK KIT received FDA 510(k) clearance on 2009-12-29, under 510(k) number K092855.

Who is the listed applicant for MILTEX MEMBRANE TACK KIT?

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

What is the FDA product code for MILTEX MEMBRANE TACK KIT?

The FDA product code for MILTEX MEMBRANE TACK KIT is DZL.

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Other records listing Miltex, Inc. as applicant

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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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