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FDA 510(k)

RIA DIAG. TEST KIT FOR INDEXING THYROX.

K-Number: K781560 · 1978-10-17

ApplicantNuclear Diagnostics, Inc.
Decision Date1978-10-17
Product CodeCEC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA DIAG. TEST KIT FOR INDEXING THYROX. is the device name listed in this FDA 510(k) record. The listed applicant is Nuclear Diagnostics, Inc.. It received FDA 510(k) clearance on 1978-10-17 under 510(k) number K781560. The device is classified under product code CEC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA DIAG. TEST KIT FOR INDEXING THYROX.?

RIA DIAG. TEST KIT FOR INDEXING THYROX. is a medical device that received FDA 510(k) clearance on 1978-10-17. The listed applicant is Nuclear Diagnostics, Inc.. The 510(k) number is K781560.

When did RIA DIAG. TEST KIT FOR INDEXING THYROX. receive FDA 510(k) clearance?

RIA DIAG. TEST KIT FOR INDEXING THYROX. received FDA 510(k) clearance on 1978-10-17, under 510(k) number K781560.

Who is the listed applicant for RIA DIAG. TEST KIT FOR INDEXING THYROX.?

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

What is the FDA product code for RIA DIAG. TEST KIT FOR INDEXING THYROX.?

The FDA product code for RIA DIAG. TEST KIT FOR INDEXING THYROX. is CEC.

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Other records listing Nuclear Diagnostics, 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.

K923917ELIPASE HUMAN PANCREATIC LIPASE ENZYMEIMMUNOASSAYK932406NUCLITRYP(TM)(I125)-HUMAN PANCREA CATH TRY RAD KITK872177TIPSEP-CORTISOL RIA DIAGNOSTIC KITK862312ENZLIPASE, ENZYMATIC LIPASE KITK860472NUCLEAR LASER ALIGNMENT SYSTEM FOR CARDIC STRESSK861735TIPSEP-TBG ASSAY

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Related Devices (Code: CEC)

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.

K240273Access Free T4Beckman Coulter, Inc.K220456Elecsys FT4 IVRoche DiagnosticsK182423MAGLUMI 2000 FT4Shenzhen New Industries Biomedical Engineering Co., Ltd.K181233Elecsys FT4 IIIRoche DiagnosticsK173122Abbott Architect Free T4Abbott LaboratoriesK152422FREND™ Free T4 Test SystemNanoentek USA, 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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