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FDA 510(k)

NML-5010/5020 MULTI-DETECTOR SYSTEM

K-Number: K832002 · 1983-08-08

ApplicantNuclear Medical Laboratories, Inc.
Decision Date1983-08-08
Product CodeJJJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NML-5010/5020 MULTI-DETECTOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nuclear Medical Laboratories, Inc.. It received FDA 510(k) clearance on 1983-08-08 under 510(k) number K832002. 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 NML-5010/5020 MULTI-DETECTOR SYSTEM?

NML-5010/5020 MULTI-DETECTOR SYSTEM is a medical device that received FDA 510(k) clearance on 1983-08-08. The listed applicant is Nuclear Medical Laboratories, Inc.. The 510(k) number is K832002.

When did NML-5010/5020 MULTI-DETECTOR SYSTEM receive FDA 510(k) clearance?

NML-5010/5020 MULTI-DETECTOR SYSTEM received FDA 510(k) clearance on 1983-08-08, under 510(k) number K832002.

Who is the listed applicant for NML-5010/5020 MULTI-DETECTOR SYSTEM?

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

What is the FDA product code for NML-5010/5020 MULTI-DETECTOR SYSTEM?

The FDA product code for NML-5010/5020 MULTI-DETECTOR SYSTEM is JJJ.

Related Clinical Trials

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Other records listing Nuclear Medical Laboratories, 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.

K852438NML TSH IRMAK844583TSH-STATK840466NML CORTISOL RIAK840589TRI-TUBE RIAK832892MODIFIED CHORIO-SHUREK823679NML 6000 CT

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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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