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FDA 510(k)

NML 6000 CT

K-Number: K823679 · 1983-01-07

ApplicantNuclear Medical Laboratories, Inc.
Decision Date1983-01-07
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NML 6000 CT 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 1983-01-07 under 510(k) number K823679. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NML 6000 CT?

NML 6000 CT is a medical device that received FDA 510(k) clearance on 1983-01-07. The listed applicant is Nuclear Medical Laboratories, Inc.. The 510(k) number is K823679.

When did NML 6000 CT receive FDA 510(k) clearance?

NML 6000 CT received FDA 510(k) clearance on 1983-01-07, under 510(k) number K823679.

Who is the listed applicant for NML 6000 CT?

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 6000 CT?

The FDA product code for NML 6000 CT is JQP.

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-SHUREK832002NML-5010/5020 MULTI-DETECTOR SYSTEM

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Related Devices (Code: JQP)

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.

K113007BIONIME DIABETES MANAGEMENT SYSTEM VI.0Bionime CorporationK983468FASTTAKE ADAPTER, MODEL # P/N 020-072-01Selfcare, Inc.K964460THE ROBOLITEShai Syg Motion and Innovations, Ltd.K953652PRENVAL IBase Ten Systems, Inc.K934111MR7000 WITH TIME MANAGER SOFTWARE (TMS)Dynatech Laboratories, Inc.K923316EXPRESSO CARTRIDGEBio-Rad Laboratories, Inc.

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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