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FDA 510(k)

LIQUISOL PROGESTERONE RADIOIMMUNO

K-Number: K820686 · 1982-04-01

ApplicantDamon Corp.
Decision Date1982-04-01
Product CodeJLS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUISOL PROGESTERONE RADIOIMMUNO is the device name listed in this FDA 510(k) record. The listed applicant is Damon Corp.. It received FDA 510(k) clearance on 1982-04-01 under 510(k) number K820686. 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 LIQUISOL PROGESTERONE RADIOIMMUNO?

LIQUISOL PROGESTERONE RADIOIMMUNO is a medical device that received FDA 510(k) clearance on 1982-04-01. The listed applicant is Damon Corp.. The 510(k) number is K820686.

When did LIQUISOL PROGESTERONE RADIOIMMUNO receive FDA 510(k) clearance?

LIQUISOL PROGESTERONE RADIOIMMUNO received FDA 510(k) clearance on 1982-04-01, under 510(k) number K820686.

Who is the listed applicant for LIQUISOL PROGESTERONE RADIOIMMUNO?

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

What is the FDA product code for LIQUISOL PROGESTERONE RADIOIMMUNO?

The FDA product code for LIQUISOL PROGESTERONE RADIOIMMUNO is JLS.

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Other records listing Damon Corp. 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.

K874865DAMON D.E.T.E.C.T IMAGE ENHANCERK831826ADRENOCORTICOTROPIN RADIO-IMMUNOASSAYK802661LIQUISOL TESTOSTERONE RADIOIMM. TEST KITK790250LIQUISOL CORTISOL RIA TEST KITK782124IEC CENTRA-7 CENTRIFUGE MODEL 2362K781012RIA TEST KIT SYS. DAMON KIQUISOL FREE

View all 11 devices →

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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