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FDA 510(k)

NOBLESCOPE NEUROENDOSCOPE SYSTEM & ACCESSORIES

K-Number: K953554 · 1995-10-18

Decision Date1995-10-18
Product CodeGWG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NOBLESCOPE NEUROENDOSCOPE SYSTEM & ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Nobles-Lai Engineering, Inc.. It received FDA 510(k) clearance on 1995-10-18 under 510(k) number K953554. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOBLESCOPE NEUROENDOSCOPE SYSTEM & ACCESSORIES?

NOBLESCOPE NEUROENDOSCOPE SYSTEM & ACCESSORIES is a medical device that received FDA 510(k) clearance on 1995-10-18. The listed applicant is Nobles-Lai Engineering, Inc.. The 510(k) number is K953554.

When did NOBLESCOPE NEUROENDOSCOPE SYSTEM & ACCESSORIES receive FDA 510(k) clearance?

NOBLESCOPE NEUROENDOSCOPE SYSTEM & ACCESSORIES received FDA 510(k) clearance on 1995-10-18, under 510(k) number K953554.

Who is the listed applicant for NOBLESCOPE NEUROENDOSCOPE SYSTEM & ACCESSORIES?

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

What is the FDA product code for NOBLESCOPE NEUROENDOSCOPE SYSTEM & ACCESSORIES?

The FDA product code for NOBLESCOPE NEUROENDOSCOPE SYSTEM & ACCESSORIES is GWG.

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 Nobles-Lai Engineering, 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: GWG)

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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