FDA 510(k)

SURGI-TIE LOOPS

K-Number: K861161 · 1986-06-10

Decision Date1986-06-10

Product Code

DecisionSubstantially Equivalent

Device Summary

SURGI-TIE LOOPS is the device name listed in this FDA 510(k) record. The listed applicant is Healthmed Corp.. It received FDA 510(k) clearance on 1986-06-10 under 510(k) number K861161. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGI-TIE LOOPS?

SURGI-TIE LOOPS is a medical device that received FDA 510(k) clearance on 1986-06-10. The listed applicant is Healthmed Corp.. The 510(k) number is K861161.

When did SURGI-TIE LOOPS receive FDA 510(k) clearance?

SURGI-TIE LOOPS received FDA 510(k) clearance on 1986-06-10, under 510(k) number K861161.

Who is the listed applicant for SURGI-TIE LOOPS?

The FDA 510(k) record lists Healthmed Corp. 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 Healthmed Corp. as applicant

K890006BAXTER STERILE TOWEL

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.