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FDA 510(k)

CHEMO-PORT

K-Number: K913386 · 1992-01-10

ApplicantHdc Corp.
Decision Date1992-01-10
Product CodeFMI
Advisory CommitteeHO
DecisionUnknown

Device Summary

CHEMO-PORT is the device name listed in this FDA 510(k) record. The listed applicant is Hdc Corp.. It received FDA 510(k) clearance on 1992-01-10 under 510(k) number K913386. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CHEMO-PORT?

CHEMO-PORT is a medical device that received FDA 510(k) clearance on 1992-01-10. The listed applicant is Hdc Corp.. The 510(k) number is K913386.

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

CHEMO-PORT received FDA 510(k) clearance on 1992-01-10, under 510(k) number K913386.

Who is the listed applicant for CHEMO-PORT?

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 CHEMO-PORT?

The FDA product code for CHEMO-PORT is FMI.

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Related Devices (Code: FMI)

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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.

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