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FDA 510(k)

L.C.S.3000

K-Number: K926464 · 1993-08-24

ApplicantCryodyne Technologies, Inc.
Decision Date1993-08-24
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

L.C.S.3000 is the device name listed in this FDA 510(k) record. The listed applicant is Cryodyne Technologies, Inc.. It received FDA 510(k) clearance on 1993-08-24 under 510(k) number K926464. 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.3000?

L.C.S.3000 is a medical device that received FDA 510(k) clearance on 1993-08-24. The listed applicant is Cryodyne Technologies, Inc.. The 510(k) number is K926464.

When did L.C.S.3000 receive FDA 510(k) clearance?

L.C.S.3000 received FDA 510(k) clearance on 1993-08-24, under 510(k) number K926464.

Who is the listed applicant for L.C.S.3000?

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

What is the FDA product code for L.C.S.3000?

The FDA product code for L.C.S.3000 is GEH.

Other records listing Cryodyne Technologies, 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.

K932520CALIBRATION GASK881465CRYOBIOLOGICAL FREEZERK881467MICROSCOPE STAGE HEATERK881466CELL-CULTURE SHAKERK860738CTC 30, 40, 1 LIQUID OXYGEN LITERS

Related Devices (Code: GEH)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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