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FDA 510(k)

LAPAROSCOPIC NEEDLE HOLDER

K-Number: K924196 · 1993-06-25

ApplicantNusurg, Inc.
Decision Date1993-06-25
Product CodeFHQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC NEEDLE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Nusurg, Inc.. It received FDA 510(k) clearance on 1993-06-25 under 510(k) number K924196. The device is classified under product code FHQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPAROSCOPIC NEEDLE HOLDER?

LAPAROSCOPIC NEEDLE HOLDER is a medical device that received FDA 510(k) clearance on 1993-06-25. The listed applicant is Nusurg, Inc.. The 510(k) number is K924196.

When did LAPAROSCOPIC NEEDLE HOLDER receive FDA 510(k) clearance?

LAPAROSCOPIC NEEDLE HOLDER received FDA 510(k) clearance on 1993-06-25, under 510(k) number K924196.

Who is the listed applicant for LAPAROSCOPIC NEEDLE HOLDER?

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

What is the FDA product code for LAPAROSCOPIC NEEDLE HOLDER?

The FDA product code for LAPAROSCOPIC NEEDLE HOLDER is FHQ.

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 Nusurg, 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.

Related Devices (Code: FHQ)

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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