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FDA 510(k)

STRYKER VISUM SURGICAL LIGHTING SYSTEM

K-Number: K031068 · 2003-08-12

ApplicantStryker Endoscopy
Decision Date2003-08-12
Product CodeFSY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STRYKER VISUM SURGICAL LIGHTING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 2003-08-12 under 510(k) number K031068. The device is classified under product code FSY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER VISUM SURGICAL LIGHTING SYSTEM?

STRYKER VISUM SURGICAL LIGHTING SYSTEM is a medical device that received FDA 510(k) clearance on 2003-08-12. The listed applicant is Stryker Endoscopy. The 510(k) number is K031068.

When did STRYKER VISUM SURGICAL LIGHTING SYSTEM receive FDA 510(k) clearance?

STRYKER VISUM SURGICAL LIGHTING SYSTEM received FDA 510(k) clearance on 2003-08-12, under 510(k) number K031068.

Who is the listed applicant for STRYKER VISUM SURGICAL LIGHTING SYSTEM?

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

What is the FDA product code for STRYKER VISUM SURGICAL LIGHTING SYSTEM?

The FDA product code for STRYKER VISUM SURGICAL LIGHTING SYSTEM is FSY.

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Related Devices (Code: FSY)

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.

K132747VISUM BLADE LED SURGICAL LIGHTING SYSTEMStryker CommunicationsK132307VIDA LED SURGICAL LIGHTING SYSTEMConvida Healthcare & Systems CorporationK131893AMICO CE SERIES SURGICAL LIGHTS, MIRA LED SERIES MINOR SURGICAL LIGHTSAjw Technology Consultants, Inc.K122875ORICARE L2700Oricare, Inc.K120392CHROMOPHARE F 628 AND F 528Berchtold GmbH & Co. KGK102758TRULIGHT 5520 AND TRULIGHT 5320Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg

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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