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FDA 510(k)

RIA KIT, PROGESTERONE

K-Number: K782009 · 1979-03-02

ApplicantThe Upjohn Co.
Decision Date1979-03-02
Product CodeJLS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA KIT, PROGESTERONE is the device name listed in this FDA 510(k) record. The listed applicant is The Upjohn Co.. It received FDA 510(k) clearance on 1979-03-02 under 510(k) number K782009. The device is classified under product code JLS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA KIT, PROGESTERONE?

RIA KIT, PROGESTERONE is a medical device that received FDA 510(k) clearance on 1979-03-02. The listed applicant is The Upjohn Co.. The 510(k) number is K782009.

When did RIA KIT, PROGESTERONE receive FDA 510(k) clearance?

RIA KIT, PROGESTERONE received FDA 510(k) clearance on 1979-03-02, under 510(k) number K782009.

Who is the listed applicant for RIA KIT, PROGESTERONE?

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

What is the FDA product code for RIA KIT, PROGESTERONE?

The FDA product code for RIA KIT, PROGESTERONE is JLS.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing The Upjohn Co. 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.

K902004TROBICIN SUSCEPTIBILITY POWDERK900455ZEFAZONE SUSCEPTIBILITY POWDERK810853CK-TOTAL/CK-B (NAC) BIOLUMIN. ASSAY KITK780792TESTOSTERONE RADIOIMMUNOASSAY KIT 125IK760920CAT-A-KIT

Related Devices (Code: JLS)

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.

K040923LUMINESCENT IMMUNOASSAY KIT FOR THE DETECTION OF PROGESTERONE IN SALIVAIbl GmbHK973898PROGESTERONE ELISAKmi Diagnostics, Inc.K972133VITROS IMMUNODIAGNOSTICS PRODUCTS PROGESTERONE REAGENT PACK (GEM.1070), PROGESTERONE CALIBRATORS (GEM.C070)Johnson & Johnson Clinical Diagnostics, Inc.K971725OPUS PROGESTERONEBehring Diagnostics, Inc.K964841ELECSYS PROGESTERONE ASSAYBoehringer Mannheim Corp.K965084VIDAS PROESTERONE (PRG) (30 409)bioMerieux, 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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