Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MEDSURG SINGLE USE BASIN SET

K-Number: K861784 · 1986-05-21

ApplicantMedsurg Industries, Inc.
Decision Date1986-05-21
Product Code
DecisionSubstantially Equivalent

Device Summary

MEDSURG SINGLE USE BASIN SET is the device name listed in this FDA 510(k) record. The listed applicant is Medsurg Industries, Inc.. It received FDA 510(k) clearance on 1986-05-21 under 510(k) number K861784. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDSURG SINGLE USE BASIN SET?

MEDSURG SINGLE USE BASIN SET is a medical device that received FDA 510(k) clearance on 1986-05-21. The listed applicant is Medsurg Industries, Inc.. The 510(k) number is K861784.

When did MEDSURG SINGLE USE BASIN SET receive FDA 510(k) clearance?

MEDSURG SINGLE USE BASIN SET received FDA 510(k) clearance on 1986-05-21, under 510(k) number K861784.

Who is the listed applicant for MEDSURG SINGLE USE BASIN SET?

The FDA 510(k) record lists Medsurg Industries, 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_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 Medsurg Industries, Inc. 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.

K920780MEDSURG INSERTION TRAYK940175MEDSURG STERILE O.R. TOWELSK934731MEDSURG STERILE IMAGING PRODUCTSK925558INFILTUBEK934971STERILE LAPAROTOMY SPONGESK920421MEDSURG MARSHMALLOW TRAY

View all 41 devices →

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.

↑