FDA 510(k)

HDC SILCATH SUBCLAVIAN CATHETER PERCUTANEOUS INSER

K-Number: K851078 · 1985-04-19

Decision Date1985-04-19

Product CodeDYB

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

HDC SILCATH SUBCLAVIAN CATHETER PERCUTANEOUS INSER is the device name listed in this FDA 510(k) record. The listed applicant is Hdc Corp.. It received FDA 510(k) clearance on 1985-04-19 under 510(k) number K851078. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HDC SILCATH SUBCLAVIAN CATHETER PERCUTANEOUS INSER?

HDC SILCATH SUBCLAVIAN CATHETER PERCUTANEOUS INSER is a medical device that received FDA 510(k) clearance on 1985-04-19. The listed applicant is Hdc Corp.. The 510(k) number is K851078.

When did HDC SILCATH SUBCLAVIAN CATHETER PERCUTANEOUS INSER receive FDA 510(k) clearance?

HDC SILCATH SUBCLAVIAN CATHETER PERCUTANEOUS INSER received FDA 510(k) clearance on 1985-04-19, under 510(k) number K851078.

Who is the listed applicant for HDC SILCATH SUBCLAVIAN CATHETER PERCUTANEOUS INSER?

The FDA 510(k) record lists Hdc Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HDC SILCATH SUBCLAVIAN CATHETER PERCUTANEOUS INSER?

The FDA product code for HDC SILCATH SUBCLAVIAN CATHETER PERCUTANEOUS INSER is DYB.

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 Hdc Corp. as applicant

K071875V-CATH POLY PICC K023342NEURO-TRACE III KIT, NEURO-TRACE III REGIONAL BLOCK CABLE, NEURO-TRACE III NERVE MAPPING PROBE, NEURO-TRACE III NERVE BG K033853MODIFICATION TO V-CATH POLY PICC K032404SELDINGER SAFETY NEEDLE INTRODUCER K022752PANDIN CONTINUOUS NERVE STIMULATING CATHETER, MODELS 561-18-05, 561-18-09, 561-18-15, 562-18-05, 562-18-09 & 562-18-15 K022099SAFE-T-PEEL SAFETY NEEDLE/INTRODUCER, MODELS 350-300 S, 360-300'S,380-300'S,390-300'S

View all 30 devices →

Related Devices (Code: DYB)

K253526NAMIC Dilator and SheathMedline Industries, LP K261529Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set/ Microintroducer Kit / Microintroducer Kit (SIS05C); Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set / Microintroducer Kit / Microintroducer Kit (IS01); Introducer Kit / Microintroducer Kit / Introducer Set /Microintroducer Set / Micro Introducer Sheath Set / Introducer Sheath Set (NIS04)Hartman Medical Group, LLC K261242SimplGuidePendracare K261950Health Line Tearaway IntroducerHealth Line International Corporation K261492FieldFlex Steerable SheathCenterPoint Systems, LLC K260606Echo Large Bore Introducer SheathEcho Medical, LLC

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.