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FDA 510(k)

BR-S601MU (SURGICAL VIDEO RECORDER)

K-Number: K890119 · 1989-01-24

ApplicantVictor Co. of Japan, Ltd. C/O Jvc Corp.
Decision Date1989-01-24
Product CodeFWC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BR-S601MU (SURGICAL VIDEO RECORDER) is the device name listed in this FDA 510(k) record. The listed applicant is Victor Co. of Japan, Ltd. C/O Jvc Corp.. It received FDA 510(k) clearance on 1989-01-24 under 510(k) number K890119. The device is classified under product code FWC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BR-S601MU (SURGICAL VIDEO RECORDER)?

BR-S601MU (SURGICAL VIDEO RECORDER) is a medical device that received FDA 510(k) clearance on 1989-01-24. The listed applicant is Victor Co. of Japan, Ltd. C/O Jvc Corp.. The 510(k) number is K890119.

When did BR-S601MU (SURGICAL VIDEO RECORDER) receive FDA 510(k) clearance?

BR-S601MU (SURGICAL VIDEO RECORDER) received FDA 510(k) clearance on 1989-01-24, under 510(k) number K890119.

Who is the listed applicant for BR-S601MU (SURGICAL VIDEO RECORDER)?

The FDA 510(k) record lists Victor Co. of Japan, Ltd. C/O Jvc Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BR-S601MU (SURGICAL VIDEO RECORDER)?

The FDA product code for BR-S601MU (SURGICAL VIDEO RECORDER) is FWC.

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Related Devices (Code: FWC)

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.

K864381LUXTEC VIDEOLUX 20/20 CAMERA HEADLIGHT SYSTEMLuxtec Corp.K854988KY-M280U SURGICAL CAMERAUs Jvc Corp.

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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