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FDA 510(k)

GENESYS 6000 GAMMA COUNTER

K-Number: K900087 · 1990-07-19

ApplicantLaboratory Technologies, Inc.
Decision Date1990-07-19
Product CodeJJJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GENESYS 6000 GAMMA COUNTER is the device name listed in this FDA 510(k) record. The listed applicant is Laboratory Technologies, Inc.. It received FDA 510(k) clearance on 1990-07-19 under 510(k) number K900087. 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 GENESYS 6000 GAMMA COUNTER?

GENESYS 6000 GAMMA COUNTER is a medical device that received FDA 510(k) clearance on 1990-07-19. The listed applicant is Laboratory Technologies, Inc.. The 510(k) number is K900087.

When did GENESYS 6000 GAMMA COUNTER receive FDA 510(k) clearance?

GENESYS 6000 GAMMA COUNTER received FDA 510(k) clearance on 1990-07-19, under 510(k) number K900087.

Who is the listed applicant for GENESYS 6000 GAMMA COUNTER?

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

What is the FDA product code for GENESYS 6000 GAMMA COUNTER?

The FDA product code for GENESYS 6000 GAMMA COUNTER is JJJ.

Related Clinical Trials

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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Other records listing Laboratory 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.

K921536ACCULYTE CHEMILUMINESCENCE ANALYZERK882194GEMINII GAMMA COUNTERK851689GENESYS GAMMA COUNTER

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 LaboratoriesK896202MATRIX(TM)-96Canberra Industries, Inc.K894902SOURCEREROakfield Instruments, Ltd.K884091SOURCERERJohn Caunt Scientific , Ltd.

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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