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FDA 510(k)

SUBCLAVIAN JUGULAR CATHETER SET

K-Number: K820102 · 1982-01-29

ApplicantLuther Medical Products, Inc.
Decision Date1982-01-29
Product CodeDQR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SUBCLAVIAN JUGULAR CATHETER SET is the device name listed in this FDA 510(k) record. The listed applicant is Luther Medical Products, Inc.. It received FDA 510(k) clearance on 1982-01-29 under 510(k) number K820102. The device is classified under product code DQR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUBCLAVIAN JUGULAR CATHETER SET?

SUBCLAVIAN JUGULAR CATHETER SET is a medical device that received FDA 510(k) clearance on 1982-01-29. The listed applicant is Luther Medical Products, Inc.. The 510(k) number is K820102.

When did SUBCLAVIAN JUGULAR CATHETER SET receive FDA 510(k) clearance?

SUBCLAVIAN JUGULAR CATHETER SET received FDA 510(k) clearance on 1982-01-29, under 510(k) number K820102.

Who is the listed applicant for SUBCLAVIAN JUGULAR CATHETER SET?

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

What is the FDA product code for SUBCLAVIAN JUGULAR CATHETER SET?

The FDA product code for SUBCLAVIAN JUGULAR CATHETER SET is DQR.

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Other records listing Luther Medical Products, 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.

K982797BLUNT T-PEEL INTRODUCER MODEL NUMBER PE-16PICB, PE-18PICB, PE-20PICB, PE-24PICBK980090ONECATH, L-CATH CATHETER SYSTEM, MODEL OC-(16-22 GA., 5CM-60CM)K974543L-CATH MODIFIED SELDINGER TECHNIQUE INSERTION/CATHETER EXCHANGE KIT PE-MST24-24 GA. KIT, L-CATH MODIFIED SELDINGERK940198L-CATH CONNECTOR ASSEMBLYK942103L-CATH CATHETER SYSTEM - PORT L-CATHK930473ONECATH L-CATH CATHETER SYSTEM

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Related Devices (Code: DQR)

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.

K131446INTEGRA JARIT HEPARIN CANNULAS, INJECTORS, AND NEEDLESIntegra LifeSciences CorporationK07355918 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA IIEdwards Lifesciences Research MedicalK051655ANGIODYNAMICS, INC., MICRO ACCESS KITSAngioDynamics, Inc.K030398CARDIACASSIST TRANSSEPTAL CANNULA SET, MODEL 5132-6221Cardiacassist, Inc.K960098RMI INTERNAL MAMMARY ARTERY CANNULAResearch Medical, Inc.K902674DATASCOPE ARTERIAL CANNULA W/ACCESS PORTDatascope Corp.

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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