FDA 510(k)

HDC CHEMO-PORT (VASCULAR)

K-Number: K853332 · 1986-07-17

Decision Date1986-07-17

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

HDC CHEMO-PORT (VASCULAR) is the device name listed in this FDA 510(k) record. The listed applicant is Hdc Corp.. It received FDA 510(k) clearance on 1986-07-17 under 510(k) number K853332. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HDC CHEMO-PORT (VASCULAR)?

HDC CHEMO-PORT (VASCULAR) is a medical device that received FDA 510(k) clearance on 1986-07-17. The listed applicant is Hdc Corp.. The 510(k) number is K853332.

When did HDC CHEMO-PORT (VASCULAR) receive FDA 510(k) clearance?

HDC CHEMO-PORT (VASCULAR) received FDA 510(k) clearance on 1986-07-17, under 510(k) number K853332.

Who is the listed applicant for HDC CHEMO-PORT (VASCULAR)?

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 HDC CHEMO-PORT (VASCULAR)?

The FDA product code for HDC CHEMO-PORT (VASCULAR) is LJT.

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Related Devices (Code: LJT)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.