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FDA 510(k)

LKB-WALLAC 1230 ARCUS FLUOROMETER

K-Number: K851984 · 1985-05-24

ApplicantLkb Instruments, Inc.
Decision Date1985-05-24
Product CodeKHO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LKB-WALLAC 1230 ARCUS FLUOROMETER is the device name listed in this FDA 510(k) record. The listed applicant is Lkb Instruments, Inc.. It received FDA 510(k) clearance on 1985-05-24 under 510(k) number K851984. The device is classified under product code KHO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LKB-WALLAC 1230 ARCUS FLUOROMETER?

LKB-WALLAC 1230 ARCUS FLUOROMETER is a medical device that received FDA 510(k) clearance on 1985-05-24. The listed applicant is Lkb Instruments, Inc.. The 510(k) number is K851984.

When did LKB-WALLAC 1230 ARCUS FLUOROMETER receive FDA 510(k) clearance?

LKB-WALLAC 1230 ARCUS FLUOROMETER received FDA 510(k) clearance on 1985-05-24, under 510(k) number K851984.

Who is the listed applicant for LKB-WALLAC 1230 ARCUS FLUOROMETER?

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

What is the FDA product code for LKB-WALLAC 1230 ARCUS FLUOROMETER?

The FDA product code for LKB-WALLAC 1230 ARCUS FLUOROMETER is KHO.

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Other records listing Lkb Instruments, Inc. as applicant

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Related Devices (Code: KHO)

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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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