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FDA 510(k)

PROCEED VENTRAL PATCH

K-Number: K061533 · 2006-12-11

ApplicantETHICON, Inc.
Decision Date2006-12-11
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROCEED VENTRAL PATCH is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 2006-12-11 under 510(k) number K061533. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROCEED VENTRAL PATCH?

PROCEED VENTRAL PATCH is a medical device that received FDA 510(k) clearance on 2006-12-11. The listed applicant is ETHICON, Inc.. The 510(k) number is K061533.

When did PROCEED VENTRAL PATCH receive FDA 510(k) clearance?

PROCEED VENTRAL PATCH received FDA 510(k) clearance on 2006-12-11, under 510(k) number K061533.

Who is the listed applicant for PROCEED VENTRAL PATCH?

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

What is the FDA product code for PROCEED VENTRAL PATCH?

The FDA product code for PROCEED VENTRAL PATCH is FTL.

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Related Devices (Code: FTL)

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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