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FDA 510(k)

LCA 2000

K-Number: K871034 · 1987-04-10

ApplicantVistek Corp.
Decision Date1987-04-10
Product CodeFTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LCA 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Vistek Corp.. It received FDA 510(k) clearance on 1987-04-10 under 510(k) number K871034. The device is classified under product code FTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LCA 2000?

LCA 2000 is a medical device that received FDA 510(k) clearance on 1987-04-10. The listed applicant is Vistek Corp.. The 510(k) number is K871034.

When did LCA 2000 receive FDA 510(k) clearance?

LCA 2000 received FDA 510(k) clearance on 1987-04-10, under 510(k) number K871034.

Who is the listed applicant for LCA 2000?

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

What is the FDA product code for LCA 2000?

The FDA product code for LCA 2000 is FTA.

Other records listing Vistek Corp. 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.

K904681VLS 5300 300W XENON LIGHT SOURCEK904682VISTEK ELECTRONIC CONTROLLERK860173VIS-2000 VIDEO SYSTEMK843806VIS-1000 VIDEO SYSTEM

Related Devices (Code: FTA)

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.

K112133OASYS SURGICAL LIGHT CONTROLLEROasys HealthcareK102791EASYSUITE SURGICAL LIGHT CONTROL (ESLC)Image Stream Medical, Inc.K081698MAINSTREAM OR SURGICAL LIGHT CONTROL (MSLC)Image Stream Medical, Inc.K053321LIGHT GUARD LIGHT HANDLE AND LIGHT HANDLE COVERXodus Medical, Inc.K051505SCB/STERIS OR-LIGHT INTERFACE BOXKARL STORZ Endoscopy-America, Inc.K023704KSEA SCB ACC CONTROLKARL STORZ Endoscopy-America, Inc.

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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