FDA 510(k)

NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT

K-Number: K863723 · 1986-10-29

Decision Date1986-10-29

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT is the device name listed in this FDA 510(k) record. The listed applicant is Norfolk Medical Products, Inc.. It received FDA 510(k) clearance on 1986-10-29 under 510(k) number K863723. 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 NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT?

NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT is a medical device that received FDA 510(k) clearance on 1986-10-29. The listed applicant is Norfolk Medical Products, Inc.. The 510(k) number is K863723.

When did NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT receive FDA 510(k) clearance?

NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT received FDA 510(k) clearance on 1986-10-29, under 510(k) number K863723.

Who is the listed applicant for NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT?

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

What is the FDA product code for NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT?

The FDA product code for NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT is LJT.

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Other records listing Norfolk Medical Products, Inc. as applicant

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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.