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FDA 510(k)

MSS-28CS-301/701 NEEDLESCOPE

K-Number: K013759 · 2002-08-20

ApplicantOlympus Optical Co., Ltd.
Decision Date2002-08-20
Product CodeGWG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MSS-28CS-301/701 NEEDLESCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Optical Co., Ltd.. It received FDA 510(k) clearance on 2002-08-20 under 510(k) number K013759. 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 MSS-28CS-301/701 NEEDLESCOPE?

MSS-28CS-301/701 NEEDLESCOPE is a medical device that received FDA 510(k) clearance on 2002-08-20. The listed applicant is Olympus Optical Co., Ltd.. The 510(k) number is K013759.

When did MSS-28CS-301/701 NEEDLESCOPE receive FDA 510(k) clearance?

MSS-28CS-301/701 NEEDLESCOPE received FDA 510(k) clearance on 2002-08-20, under 510(k) number K013759.

Who is the listed applicant for MSS-28CS-301/701 NEEDLESCOPE?

The FDA 510(k) record lists Olympus Optical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MSS-28CS-301/701 NEEDLESCOPE?

The FDA product code for MSS-28CS-301/701 NEEDLESCOPE is GWG.

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Other records listing Olympus Optical Co., Ltd. as applicant

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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.

K253602Precision S 4K SinuscopeStryker EndoscopyK253679Hydro Irrigation SystemStryker InstrumentsK243429HJY VisualNext 3D Endoscopic Vision SystemHjy Smart Medical Device Co., Ltd.K250752AURORA® Surgiscope® System (ASX15/60); AURORA® Surgiscope® System (ASX15/80)Integra LifeSciences CorporationK233391cCeLL - In vivoVPIX Medical, Inc.K223615Digital ClarusScope System, Digital NeuroPEN SystemClarus Medical, LLC

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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