FDA 510(k)

THE SUTURER

K-Number: K842912 · 1984-08-15

Decision Date1984-08-15

Product Code

DecisionSubstantially Equivalent

Device Summary

THE SUTURER is the device name listed in this FDA 510(k) record. The listed applicant is Vlm Surgical, Inc.. It received FDA 510(k) clearance on 1984-08-15 under 510(k) number K842912. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE SUTURER?

THE SUTURER is a medical device that received FDA 510(k) clearance on 1984-08-15. The listed applicant is Vlm Surgical, Inc.. The 510(k) number is K842912.

When did THE SUTURER receive FDA 510(k) clearance?

THE SUTURER received FDA 510(k) clearance on 1984-08-15, under 510(k) number K842912.

Who is the listed applicant for THE SUTURER?

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

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Vlm Surgical, Inc. as applicant

K945949KILEJIAN CIRCUMCISION TEMPLATE [THE DOME]

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.