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FDA 510(k)

NORFOLK MEDICAL PERITONEAL-ACCESS PORT

K-Number: K854593 · 1986-02-04

Decision Date1986-02-04
Product CodeLMQ
DecisionSubstantially Equivalent

Device Summary

NORFOLK MEDICAL PERITONEAL-ACCESS PORT 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 1986-02-04 under 510(k) number K854593. The device is classified under product code LMQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORFOLK MEDICAL PERITONEAL-ACCESS PORT?

NORFOLK MEDICAL PERITONEAL-ACCESS PORT is a medical device that received FDA 510(k) clearance on 1986-02-04. The listed applicant is Norfolk Medical Products, Inc.. The 510(k) number is K854593.

When did NORFOLK MEDICAL PERITONEAL-ACCESS PORT receive FDA 510(k) clearance?

NORFOLK MEDICAL PERITONEAL-ACCESS PORT received FDA 510(k) clearance on 1986-02-04, under 510(k) number K854593.

Who is the listed applicant for NORFOLK MEDICAL PERITONEAL-ACCESS PORT?

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 MEDICAL PERITONEAL-ACCESS PORT?

The FDA product code for NORFOLK MEDICAL PERITONEAL-ACCESS PORT is LMQ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Norfolk Medical Products, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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