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FDA 510(k)

NORFOLK MEDICAL POSI-GRIP 'HUBER POINT' NEEDLE

K-Number: K863721 · 1986-10-14

ApplicantNorfolk Medical Products, Inc.
Decision Date1986-10-14
Product Code
DecisionSubstantially Equivalent

Device Summary

NORFOLK MEDICAL POSI-GRIP 'HUBER POINT' NEEDLE 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 1986-10-14 under 510(k) number K863721. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORFOLK MEDICAL POSI-GRIP 'HUBER POINT' NEEDLE?

NORFOLK MEDICAL POSI-GRIP 'HUBER POINT' NEEDLE is a medical device that received FDA 510(k) clearance on 1986-10-14. The listed applicant is Norfolk Medical Products, Inc.. The 510(k) number is K863721.

When did NORFOLK MEDICAL POSI-GRIP 'HUBER POINT' NEEDLE receive FDA 510(k) clearance?

NORFOLK MEDICAL POSI-GRIP 'HUBER POINT' NEEDLE received FDA 510(k) clearance on 1986-10-14, under 510(k) number K863721.

Who is the listed applicant for NORFOLK MEDICAL POSI-GRIP 'HUBER POINT' NEEDLE?

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

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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.

K192291TidalPort-AP Implantable Apheresis Vascular Access PortK112713NORFOLK MEDICAL-SPORTPORT-FAMILY OF PORTSK102385NORFOLK MEDICAL NORPORT FAMILY OF PORTSK942784NORFOLK OMEGA PORT-LP SUBCUTANEOUSLY IMPLANTEDK896544MD2 PERSONAL INFUSION SYSTEMK872838NORFOLK NORPORT (TM) -SP (SKIN PARALLEL)

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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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