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FDA 510(k)

SILCATH CENTRAL CATHETER TRAY W/18 GA

K-Number: K831453 · 1983-07-28

ApplicantArgon Medical Corp.
Decision Date1983-07-28
Product CodeJCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SILCATH CENTRAL CATHETER TRAY W/18 GA is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Corp.. It received FDA 510(k) clearance on 1983-07-28 under 510(k) number K831453. The device is classified under product code JCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILCATH CENTRAL CATHETER TRAY W/18 GA?

SILCATH CENTRAL CATHETER TRAY W/18 GA is a medical device that received FDA 510(k) clearance on 1983-07-28. The listed applicant is Argon Medical Corp.. The 510(k) number is K831453.

When did SILCATH CENTRAL CATHETER TRAY W/18 GA receive FDA 510(k) clearance?

SILCATH CENTRAL CATHETER TRAY W/18 GA received FDA 510(k) clearance on 1983-07-28, under 510(k) number K831453.

Who is the listed applicant for SILCATH CENTRAL CATHETER TRAY W/18 GA?

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

What is the FDA product code for SILCATH CENTRAL CATHETER TRAY W/18 GA?

The FDA product code for SILCATH CENTRAL CATHETER TRAY W/18 GA is JCY.

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Other records listing Argon Medical Corp. as applicant

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Related Devices (Code: JCY)

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.

K863982VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAYVas-Cath of Canada , Ltd.K840324SILICONE SUMP DRAIN 20 & 40 FRENCHSuperior Plastic Products Corp.K834615TRIPLE LUMEN INFUSIONCATHETERS-Medical Components, Inc.K831451SILCATH CENTRAL CATHETER TRAY SIZE-Argon Medical Corp.K822096CHEMOTHERAPY INFUSION CATHETERAmerican Heyer SchulteK813606SILICONE ELASTOMER INFUSION CATHETERQuest Medical, 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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