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FDA 510(k)

RIA OF PROGESTERONE

K-Number: K790911 · 1979-06-27

ApplicantCalbiochem-Behring Corp.
Decision Date1979-06-27
Product CodeJLS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA OF PROGESTERONE is the device name listed in this FDA 510(k) record. The listed applicant is Calbiochem-Behring Corp.. It received FDA 510(k) clearance on 1979-06-27 under 510(k) number K790911. 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 OF PROGESTERONE?

RIA OF PROGESTERONE is a medical device that received FDA 510(k) clearance on 1979-06-27. The listed applicant is Calbiochem-Behring Corp.. The 510(k) number is K790911.

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

RIA OF PROGESTERONE received FDA 510(k) clearance on 1979-06-27, under 510(k) number K790911.

Who is the listed applicant for RIA OF PROGESTERONE?

The FDA 510(k) record lists Calbiochem-Behring Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIA OF PROGESTERONE?

The FDA product code for RIA OF PROGESTERONE is JLS.

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Other records listing Calbiochem-Behring Corp. as applicant

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K831811REVOLUTION RADIAL IMMUNODIFFUSION PLATEK831036ENA TEST KIT SM & RNP AUTO ANTIBODYK830214AFT SYSTEM IIIK820812CREATINE KINASE-MB KITK813493ENZYGNOST TM RUBELLA IGMK820088AFT SYSTEM PROFICIENCY TESTING PROGRAM

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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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