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FDA 510(k)

PUNCTURENEEDLE

K-Number: K963794 · 1998-03-19

ApplicantFerguson Medical
Decision Date1998-03-19
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PUNCTURENEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1998-03-19 under 510(k) number K963794. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PUNCTURENEEDLE?

PUNCTURENEEDLE is a medical device that received FDA 510(k) clearance on 1998-03-19. The listed applicant is Ferguson Medical. The 510(k) number is K963794.

When did PUNCTURENEEDLE receive FDA 510(k) clearance?

PUNCTURENEEDLE received FDA 510(k) clearance on 1998-03-19, under 510(k) number K963794.

Who is the listed applicant for PUNCTURENEEDLE?

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

What is the FDA product code for PUNCTURENEEDLE?

The FDA product code for PUNCTURENEEDLE is KNW.

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Other records listing Ferguson Medical 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.

K033153DICOM THEATERK962615TUMORLOCALIZER MRIK971813EMBLAK972217ORTHOPEDIC SCREW SYSTEMK972219ORTHOPEDIC PLATE SYSTEMK970819TARGOBEAM

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Related Devices (Code: KNW)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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