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FDA 510(k)

L.C.S. 2000 SYSTEM

K-Number: K914591 · 1992-01-14

ApplicantStiefel Research Institute, Inc.
Decision Date1992-01-14
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

L.C.S. 2000 SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stiefel Research Institute, Inc.. It received FDA 510(k) clearance on 1992-01-14 under 510(k) number K914591. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the L.C.S. 2000 SYSTEM?

L.C.S. 2000 SYSTEM is a medical device that received FDA 510(k) clearance on 1992-01-14. The listed applicant is Stiefel Research Institute, Inc.. The 510(k) number is K914591.

When did L.C.S. 2000 SYSTEM receive FDA 510(k) clearance?

L.C.S. 2000 SYSTEM received FDA 510(k) clearance on 1992-01-14, under 510(k) number K914591.

Who is the listed applicant for L.C.S. 2000 SYSTEM?

The FDA 510(k) record lists Stiefel Research Institute, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for L.C.S. 2000 SYSTEM?

The FDA product code for L.C.S. 2000 SYSTEM is GEH.

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Other records listing Stiefel Research Institute, Inc. 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.

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Official Source

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