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FDA 510(k)

PARIETEX

K-Number: K982532 · 1999-01-20

ApplicantCogent
Decision Date1999-01-20
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PARIETEX is the device name listed in this FDA 510(k) record. The listed applicant is Cogent. It received FDA 510(k) clearance on 1999-01-20 under 510(k) number K982532. 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 PARIETEX?

PARIETEX is a medical device that received FDA 510(k) clearance on 1999-01-20. The listed applicant is Cogent. The 510(k) number is K982532.

When did PARIETEX receive FDA 510(k) clearance?

PARIETEX received FDA 510(k) clearance on 1999-01-20, under 510(k) number K982532.

Who is the listed applicant for PARIETEX?

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

What is the FDA product code for PARIETEX?

The FDA product code for PARIETEX 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.

K253956ProGrip™ advanced self-gripping polypropylene mesh (ADG1510, ADG2015, ADG3020, ADG4030)Sofradim ProductionK253125Parietene™ Flat Sheet MeshMedtronic - Sofradim ProductionK251955Onflex™ MeshDavol Inc., Subsidiary of C. R. Bard, Inc.K251557Bard® Mesh; Bard® Mesh Pre-ShapedDavol, Inc.K250869Parietene™ Macroporous Mesh (PPM5050 )Sofradim ProductionK250098Bard Soft Mesh; Bard Soft Mesh Pre-ShapedDavol, Inc.

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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