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FDA 510(k)

ND1200 RIA COUNTER

K-Number: K841352 · 1984-05-02

ApplicantNuclear Data, Inc.
Decision Date1984-05-02
Product CodeJJJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ND1200 RIA COUNTER is the device name listed in this FDA 510(k) record. The listed applicant is Nuclear Data, Inc.. It received FDA 510(k) clearance on 1984-05-02 under 510(k) number K841352. 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 ND1200 RIA COUNTER?

ND1200 RIA COUNTER is a medical device that received FDA 510(k) clearance on 1984-05-02. The listed applicant is Nuclear Data, Inc.. The 510(k) number is K841352.

When did ND1200 RIA COUNTER receive FDA 510(k) clearance?

ND1200 RIA COUNTER received FDA 510(k) clearance on 1984-05-02, under 510(k) number K841352.

Who is the listed applicant for ND1200 RIA COUNTER?

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

What is the FDA product code for ND1200 RIA COUNTER?

The FDA product code for ND1200 RIA COUNTER is JJJ.

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Other records listing Nuclear Data, 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.

K891466ACCUSPEC THYROID UPTAKE SYSTEMK881383ND1100 BONE DENSITY SCANNERK844835ND2100 SPINE SCANNERK844766ND1100 BONE DENSITY SCANNERK843349ND3100 VIDEO IMAGERK841440ND62T THYROID UPTAKE SYSTEM

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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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