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FDA 510(k)

EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY)

K-Number: K010425 · 2001-03-15

ApplicantHdc Corp.
Decision Date2001-03-15
Product CodeKNF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY) is the device name listed in this FDA 510(k) record. The listed applicant is Hdc Corp.. It received FDA 510(k) clearance on 2001-03-15 under 510(k) number K010425. The device is classified under product code KNF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY)?

EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY) is a medical device that received FDA 510(k) clearance on 2001-03-15. The listed applicant is Hdc Corp.. The 510(k) number is K010425.

When did EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY) receive FDA 510(k) clearance?

EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY) received FDA 510(k) clearance on 2001-03-15, under 510(k) number K010425.

Who is the listed applicant for EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY)?

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 EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY)?

The FDA product code for EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY) is KNF.

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Other records listing Hdc Corp. 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.

K071875V-CATH POLY PICCK023342NEURO-TRACE III KIT, NEURO-TRACE III REGIONAL BLOCK CABLE, NEURO-TRACE III NERVE MAPPING PROBE, NEURO-TRACE III NERVE BGK033853MODIFICATION TO V-CATH POLY PICCK032404SELDINGER SAFETY NEEDLE INTRODUCERK022752PANDIN CONTINUOUS NERVE STIMULATING CATHETER, MODELS 561-18-05, 561-18-09, 561-18-15, 562-18-05, 562-18-09 & 562-18-15K022099SAFE-T-PEEL SAFETY NEEDLE/INTRODUCER, MODELS 350-300 S, 360-300'S,380-300'S,390-300'S

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Related Devices (Code: KNF)

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.

K254303KARL STORZ SUPRALOOPKarl Storz SE & CO. KGK250705Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K240503Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K233848Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-220)Gynesonics, Inc.K222304Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K211535Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, 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.

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