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FDA 510(k)

B-NEOCEPT 30

K-Number: K840650 · 1984-04-04

ApplicantOrganon, Inc.
Decision Date1984-04-04
Product CodeJHJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

B-NEOCEPT 30 is the device name listed in this FDA 510(k) record. The listed applicant is Organon, Inc.. It received FDA 510(k) clearance on 1984-04-04 under 510(k) number K840650. The device is classified under product code JHJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the B-NEOCEPT 30?

B-NEOCEPT 30 is a medical device that received FDA 510(k) clearance on 1984-04-04. The listed applicant is Organon, Inc.. The 510(k) number is K840650.

When did B-NEOCEPT 30 receive FDA 510(k) clearance?

B-NEOCEPT 30 received FDA 510(k) clearance on 1984-04-04, under 510(k) number K840650.

Who is the listed applicant for B-NEOCEPT 30?

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

What is the FDA product code for B-NEOCEPT 30?

The FDA product code for B-NEOCEPT 30 is JHJ.

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Other records listing Organon, 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.

K950861RECONSTITUTION ACCESSOREISK853388MONOSTICON UNI-DOTK842314DUOCLON COLOR-CEPTK841525OREIA II B-HCG PREGNANCY TEST KITK841602ACCURATE BETA 30 PREGNANCY TEST KITK832801OREIA II B-HCG, ENZYME INNUNOASSAY

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Related Devices (Code: JHJ)

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.

K972606PREGNACOL PREGNANCY TESTImmunostics Inc.,K921968IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TESTTech-Co, Inc.K935863SAS(TM) DIRECT MONOCLONAL HCGSa Scientific, Inc.K926112ACCUTEX BETA-HCG TESTJ.S. Medical Assoc.K930609SAS(TM) MONOCLONAL HCG-SLIDESa Scientific, Inc.K920716DIRECT PREGNANCY TESTTech-Co, 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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