FDA 510(k)

PRESSURE MONITORING LINES

K-Number: K802326 · 1980-10-10

Decision Date1980-10-10

Product CodeDRI

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

PRESSURE MONITORING LINES is the device name listed in this FDA 510(k) record. The listed applicant is Stanco Medical, Inc.. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K802326. The device is classified under product code DRI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE MONITORING LINES?

PRESSURE MONITORING LINES is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is Stanco Medical, Inc.. The 510(k) number is K802326.

When did PRESSURE MONITORING LINES receive FDA 510(k) clearance?

PRESSURE MONITORING LINES received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802326.

Who is the listed applicant for PRESSURE MONITORING LINES?

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

What is the FDA product code for PRESSURE MONITORING LINES?

The FDA product code for PRESSURE MONITORING LINES is DRI.

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 Stanco Medical, Inc. as applicant

K810642ATRIAL-VENTRICULAR PACING ELECTRODE KIT K810643UNIVERSAL PACING ELECTRODE KIT K802289PERICARDIOCENTESIS KIT K802287RIGHT ATRIAL LINE KIT K802288SWAN GANZ CATHETER PLACEMENT KIT K802259TRANSVENOUS PACEMAKER ELECTRODE KIT

View all 19 devices →

Related Devices (Code: DRI)

K902492CARDIOCAP II MONITORS: CH, CH-2, CH-S, CH-2SDatex Division Instrumentarium Corp.K902493CARDIOCAP II CG-2GS, 2G, 1GS, 1G, 2CG, CS MONITORDatex Division Instrumentarium Corp.K822316HEART MONITOR BRACELET ALARMHmba

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.