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FDA 510(k)

DEVICE CONNECTORS #000299-000 3/8 X 3/8 X 3/8 Y

K-Number: K870477 · 1987-04-03

ApplicantClinical Connections, Inc.
Decision Date1987-04-03
Product Code
DecisionSubstantially Equivalent

Device Summary

DEVICE CONNECTORS #000299-000 3/8 X 3/8 X 3/8 Y is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Connections, Inc.. It received FDA 510(k) clearance on 1987-04-03 under 510(k) number K870477. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEVICE CONNECTORS #000299-000 3/8 X 3/8 X 3/8 Y?

DEVICE CONNECTORS #000299-000 3/8 X 3/8 X 3/8 Y is a medical device that received FDA 510(k) clearance on 1987-04-03. The listed applicant is Clinical Connections, Inc.. The 510(k) number is K870477.

When did DEVICE CONNECTORS #000299-000 3/8 X 3/8 X 3/8 Y receive FDA 510(k) clearance?

DEVICE CONNECTORS #000299-000 3/8 X 3/8 X 3/8 Y received FDA 510(k) clearance on 1987-04-03, under 510(k) number K870477.

Who is the listed applicant for DEVICE CONNECTORS #000299-000 3/8 X 3/8 X 3/8 Y?

The FDA 510(k) record lists Clinical Connections, 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 Clinical Connections, 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.

K884435RESUBMITTED 1,3 & 4 WAY STOPCOCKS, VARIOUS PARTSK871540SWIVEL CONNECTORS #014452/#014453/#014459-120K870325#014160-TAB TUBING ROTATOR ADAPTORK870912T-CONNECTORS 014500/014501/014502/014503-120K870913INJECTION SITE #014456-120K870324#014460-120 3-WAY & #014461-120 4-WAY STOPCOCK

View all 10 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.

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