FDA 510(k)

VENTRALIGHT ST MESH WITH ECHO PS POSITIONING SYSTEM

K-Number: K130968 · 2013-05-01

Decision Date2013-05-01

Product CodeFTL

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VENTRALIGHT ST MESH WITH ECHO PS POSITIONING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2013-05-01 under 510(k) number K130968. 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 VENTRALIGHT ST MESH WITH ECHO PS POSITIONING SYSTEM?

VENTRALIGHT ST MESH WITH ECHO PS POSITIONING SYSTEM is a medical device that received FDA 510(k) clearance on 2013-05-01. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K130968.

When did VENTRALIGHT ST MESH WITH ECHO PS POSITIONING SYSTEM receive FDA 510(k) clearance?

VENTRALIGHT ST MESH WITH ECHO PS POSITIONING SYSTEM received FDA 510(k) clearance on 2013-05-01, under 510(k) number K130968.

Who is the listed applicant for VENTRALIGHT ST MESH WITH ECHO PS POSITIONING SYSTEM?

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

What is the FDA product code for VENTRALIGHT ST MESH WITH ECHO PS POSITIONING SYSTEM?

The FDA product code for VENTRALIGHT ST MESH WITH ECHO PS POSITIONING SYSTEM is FTL.

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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.