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FDA 510(k)

LS 5800 SERIES LIQUID SCINTILLATION

K-Number: K813472 · 1981-12-29

ApplicantBeckman Instruments, Inc.
Decision Date1981-12-29
Product CodeJJJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LS 5800 SERIES LIQUID SCINTILLATION is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1981-12-29 under 510(k) number K813472. The device is classified under product code JJJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LS 5800 SERIES LIQUID SCINTILLATION?

LS 5800 SERIES LIQUID SCINTILLATION is a medical device that received FDA 510(k) clearance on 1981-12-29. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K813472.

When did LS 5800 SERIES LIQUID SCINTILLATION receive FDA 510(k) clearance?

LS 5800 SERIES LIQUID SCINTILLATION received FDA 510(k) clearance on 1981-12-29, under 510(k) number K813472.

Who is the listed applicant for LS 5800 SERIES LIQUID SCINTILLATION?

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

What is the FDA product code for LS 5800 SERIES LIQUID SCINTILLATION?

The FDA product code for LS 5800 SERIES LIQUID SCINTILLATION is JJJ.

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Other records listing Beckman Instruments, Inc. as applicant

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Related Devices (Code: JJJ)

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.

K962762SEQUENTIAL SAMPLE MULTI-PHOTON DETECTORBiotraces, Inc.K946387CAPRA (CAPRAC-R) WIPETEST AND WELL COUNTERCapintec, Inc.K920559ABBOTT VERTEX ANALYZERAbbott LaboratoriesK900087GENESYS 6000 GAMMA COUNTERLaboratory Technologies, Inc.K896202MATRIX(TM)-96Canberra Industries, Inc.K894902SOURCEREROakfield Instruments, Ltd.

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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