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FDA 510(k)

HERNIAMESH T-SLING

K-Number: K020652 · 2002-05-15

ApplicantHerniamesh
Decision Date2002-05-15
Product CodePAH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HERNIAMESH T-SLING is the device name listed in this FDA 510(k) record. The listed applicant is Herniamesh. It received FDA 510(k) clearance on 2002-05-15 under 510(k) number K020652. The device is classified under product code PAH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HERNIAMESH T-SLING?

HERNIAMESH T-SLING is a medical device that received FDA 510(k) clearance on 2002-05-15. The listed applicant is Herniamesh. The 510(k) number is K020652.

When did HERNIAMESH T-SLING receive FDA 510(k) clearance?

HERNIAMESH T-SLING received FDA 510(k) clearance on 2002-05-15, under 510(k) number K020652.

Who is the listed applicant for HERNIAMESH T-SLING?

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

What is the FDA product code for HERNIAMESH T-SLING?

The FDA product code for HERNIAMESH T-SLING is PAH.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Herniamesh as applicant

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.

K973955HERNIAMESH SURGICAL MESHES

Related Devices (Code: PAH)

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.

K242473Altis Single Incision Sling System (519650); Aris Transobturator Sling System (519551); Supris Retropubic Sling System (519562)Coloplast Corp.K221874Altis Single Incision Sling SystemColoplast A/SK191416Desara One Single Incision Sling System, 1 Pack ; Desara One Single Incision Sling System, 3 PackCaldera Medical, Inc.K121562ALTIS SINGLE INCISION CLING SYSTEMColoplast A/SK123179AJUST HELICAL ADJUSTABLE SINGLE-INCISION SLINGC.R. Bard, Inc.K121641MINIARC PRO SINGLE-INCISION SLING SYSTEMAmerican Medical Systems

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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