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FDA 510(k)

MEDSURG POTT-COURNAND NEEDLE

K-Number: K854293 · 1986-01-15

ApplicantMedsurg Industries, Inc.
Decision Date1986-01-15
Product CodeDRC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDSURG POTT-COURNAND NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Medsurg Industries, Inc.. It received FDA 510(k) clearance on 1986-01-15 under 510(k) number K854293. The device is classified under product code DRC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDSURG POTT-COURNAND NEEDLE?

MEDSURG POTT-COURNAND NEEDLE is a medical device that received FDA 510(k) clearance on 1986-01-15. The listed applicant is Medsurg Industries, Inc.. The 510(k) number is K854293.

When did MEDSURG POTT-COURNAND NEEDLE receive FDA 510(k) clearance?

MEDSURG POTT-COURNAND NEEDLE received FDA 510(k) clearance on 1986-01-15, under 510(k) number K854293.

Who is the listed applicant for MEDSURG POTT-COURNAND NEEDLE?

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

What is the FDA product code for MEDSURG POTT-COURNAND NEEDLE?

The FDA product code for MEDSURG POTT-COURNAND NEEDLE is DRC.

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Other records listing Medsurg Industries, 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.

K920780MEDSURG INSERTION TRAYK940175MEDSURG STERILE O.R. TOWELSK934731MEDSURG STERILE IMAGING PRODUCTSK925558INFILTUBEK934971STERILE LAPAROTOMY SPONGESK920421MEDSURG MARSHMALLOW TRAY

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Related Devices (Code: DRC)

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.

K240246Accusafe Transseptal Guidewire (GTR31180, GTR31230)Synaptic Medical CorporationK241042SafeSharp Transseptal Needle (CLICK071, CLICK171, CLICK098, CLICK198)Pressure Products Medical Device Manufacturing, LLCK221707SafeSept® Transseptal Guidewire (SS-140)Pressure Products Medical Device Manufacturing, LLCK212625PathBuilder Transseptal NeedleShanghai Microport EP Medtech Co., Ltd.K210328SafeSept Blunt NeedlePressure Products Medical Device Manufacturing, LLCK172950TSN Transseptal NeedlePressure Products Medical Device Manufacturing, 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.

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