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FDA 510(k)

MPS HUBER NEEDLE EXTENSION SET

K-Number: K982047 · 1998-07-21

Decision Date1998-07-21
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MPS HUBER NEEDLE EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Medical Product Specialists. It received FDA 510(k) clearance on 1998-07-21 under 510(k) number K982047. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MPS HUBER NEEDLE EXTENSION SET?

MPS HUBER NEEDLE EXTENSION SET is a medical device that received FDA 510(k) clearance on 1998-07-21. The listed applicant is Medical Product Specialists. The 510(k) number is K982047.

When did MPS HUBER NEEDLE EXTENSION SET receive FDA 510(k) clearance?

MPS HUBER NEEDLE EXTENSION SET received FDA 510(k) clearance on 1998-07-21, under 510(k) number K982047.

Who is the listed applicant for MPS HUBER NEEDLE EXTENSION SET?

The FDA 510(k) record lists Medical Product Specialists as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MPS HUBER NEEDLE EXTENSION SET?

The FDA product code for MPS HUBER NEEDLE EXTENSION SET is FPA.

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 Medical Product Specialists 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.

Related Devices (Code: FPA)

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.

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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