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)

TUBING CONNECTOR #10-810-60 100/PKG NON-STERILE

K-Number: K862722 · 1986-08-11

ApplicantMercury Enterprises, Inc.
Decision Date1986-08-11
Product CodeFKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TUBING CONNECTOR #10-810-60 100/PKG NON-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Mercury Enterprises, Inc.. It received FDA 510(k) clearance on 1986-08-11 under 510(k) number K862722. The device is classified under product code FKY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBING CONNECTOR #10-810-60 100/PKG NON-STERILE?

TUBING CONNECTOR #10-810-60 100/PKG NON-STERILE is a medical device that received FDA 510(k) clearance on 1986-08-11. The listed applicant is Mercury Enterprises, Inc.. The 510(k) number is K862722.

When did TUBING CONNECTOR #10-810-60 100/PKG NON-STERILE receive FDA 510(k) clearance?

TUBING CONNECTOR #10-810-60 100/PKG NON-STERILE received FDA 510(k) clearance on 1986-08-11, under 510(k) number K862722.

Who is the listed applicant for TUBING CONNECTOR #10-810-60 100/PKG NON-STERILE?

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

What is the FDA product code for TUBING CONNECTOR #10-810-60 100/PKG NON-STERILE?

The FDA product code for TUBING CONNECTOR #10-810-60 100/PKG NON-STERILE is FKY.

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 Mercury Enterprises, 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.

K885342GENNY DENNY IV SHIELDK871789INTECARE PEDIATRIC URINE COLLECTOR

Related Devices (Code: FKY)

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.

K991003PUMP SEGMENT RINSE LINE W/ SLIP-ON CONNECTOR, PUMP SEGMENT RINSE LINE W/ LUER-LOCK CONNECTOR, T-CONNECTOR, SHORT, W/ SLIDayspring Medical, Inc.K830002CAPD COLOR-GUARD SYSTEM PREPKITAbbott LaboratoriesK771428TENCKHOFF PERITONEAL TUBING ADAPT.Quinton, Inc.

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.

↑