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FDA 510(k)

1205 BETAPLATE LIQUID SCINTILLATION COUNTER

K-Number: K874094 · 1987-11-04

ApplicantLkb Instruments, Inc.
Decision Date1987-11-04
Product CodeJJJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

1205 BETAPLATE LIQUID SCINTILLATION COUNTER 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 1987-11-04 under 510(k) number K874094. 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 1205 BETAPLATE LIQUID SCINTILLATION COUNTER?

1205 BETAPLATE LIQUID SCINTILLATION COUNTER is a medical device that received FDA 510(k) clearance on 1987-11-04. The listed applicant is Lkb Instruments, Inc.. The 510(k) number is K874094.

When did 1205 BETAPLATE LIQUID SCINTILLATION COUNTER receive FDA 510(k) clearance?

1205 BETAPLATE LIQUID SCINTILLATION COUNTER received FDA 510(k) clearance on 1987-11-04, under 510(k) number K874094.

Who is the listed applicant for 1205 BETAPLATE LIQUID SCINTILLATION COUNTER?

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 1205 BETAPLATE LIQUID SCINTILLATION COUNTER?

The FDA product code for 1205 BETAPLATE LIQUID SCINTILLATION COUNTER is JJJ.

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Other records listing Lkb Instruments, 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.

K872955DELFIA(TM) FERRITIN KITK871303DELFIA(TM) THYROXINE (T4) KITK871599DELFIA(TM) HIGE KITK871644DELFIA (TM) HTSH KITK864452DELFIA(TM) TRIIODOTHYRONINE (T3) KITK864733LKB 2260 MACROTOME

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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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