FDA 510(k)

NORFOLK OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTED

K-Number: K942784 · 1995-05-02

Decision Date1995-05-02

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

NORFOLK OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTED 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 1995-05-02 under 510(k) number K942784. 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 OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTED?

NORFOLK OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTED is a medical device that received FDA 510(k) clearance on 1995-05-02. The listed applicant is Norfolk Medical Products, Inc.. The 510(k) number is K942784.

When did NORFOLK OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTED receive FDA 510(k) clearance?

NORFOLK OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTED received FDA 510(k) clearance on 1995-05-02, under 510(k) number K942784.

Who is the listed applicant for NORFOLK OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTED?

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 OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTED?

The FDA product code for NORFOLK OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTED 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.