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FDA 510(k)

LS SERIES 200 FLOVISION SYSTEM

K-Number: K971981 · 1998-12-22

ApplicantSystam
Decision Date1998-12-22
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LS SERIES 200 FLOVISION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Systam. It received FDA 510(k) clearance on 1998-12-22 under 510(k) number K971981. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LS SERIES 200 FLOVISION SYSTEM?

LS SERIES 200 FLOVISION SYSTEM is a medical device that received FDA 510(k) clearance on 1998-12-22. The listed applicant is Systam. The 510(k) number is K971981.

When did LS SERIES 200 FLOVISION SYSTEM receive FDA 510(k) clearance?

LS SERIES 200 FLOVISION SYSTEM received FDA 510(k) clearance on 1998-12-22, under 510(k) number K971981.

Who is the listed applicant for LS SERIES 200 FLOVISION SYSTEM?

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

What is the FDA product code for LS SERIES 200 FLOVISION SYSTEM?

The FDA product code for LS SERIES 200 FLOVISION SYSTEM is CAF.

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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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