FDA 510(k)

SILCATH

K-Number: K834091 · 1984-03-06

Decision Date1984-03-06

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SILCATH is the device name listed in this FDA 510(k) record. The listed applicant is Hdc Corp.. It received FDA 510(k) clearance on 1984-03-06 under 510(k) number K834091. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILCATH?

SILCATH is a medical device that received FDA 510(k) clearance on 1984-03-06. The listed applicant is Hdc Corp.. The 510(k) number is K834091.

When did SILCATH receive FDA 510(k) clearance?

SILCATH received FDA 510(k) clearance on 1984-03-06, under 510(k) number K834091.

Who is the listed applicant for SILCATH?

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 SILCATH?

The FDA product code for SILCATH is LJS.

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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

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Related Devices (Code: LJS)

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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.