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FDA 510(k)

COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSH

K-Number: K844066 · 1985-01-18

ApplicantClinetics Corp.
Decision Date1985-01-18
Product CodeCGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSH is the device name listed in this FDA 510(k) record. The listed applicant is Clinetics Corp.. It received FDA 510(k) clearance on 1985-01-18 under 510(k) number K844066. The device is classified under product code CGJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSH?

COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSH is a medical device that received FDA 510(k) clearance on 1985-01-18. The listed applicant is Clinetics Corp.. The 510(k) number is K844066.

When did COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSH receive FDA 510(k) clearance?

COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSH received FDA 510(k) clearance on 1985-01-18, under 510(k) number K844066.

Who is the listed applicant for COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSH?

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

What is the FDA product code for COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSH?

The FDA product code for COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSH is CGJ.

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Other records listing Clinetics 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.

K862180MODIFIED COTROPIN RADIOIMMUNOASSAY KITK841580TSH RECEPTOR ANTIBODY KIT 125I TSHK833934ADRENOCORTICOTROPIC HORMONE TESTK830357RADIOIMMUNOASSAY IMMUNOGLOBULINS D.EK823380125-I LH RADIOIMMUNOASSAY KITK823379125-I FSH RADIOIMMUNOASSAY KIT

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Related Devices (Code: CGJ)

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.

K052662ONE STEP FSH MENOPAUSAL TESTInd Diagnostic, Inc.K043599MOMENTS MENOPAUSE CHECK, MODEL 9113Phamatech, Inc.K041165FSH MENOPAUSE PREDICTOR TESTACON Laboratories, Inc.K040575PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112Phamatech, Inc.K030058EARLYDETECT MENOPAUSE TEST FOR FSHEarly Detect, Inc.K002450GENUA MENOPAUSE MONITOR TEST KITGenua 1944, 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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