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FDA 510(k)

MICROMEDIC COMBOSTAT LH/FSH KIT

K-Number: K872309 · 1987-07-31

ApplicantMicromedic Systems
Decision Date1987-07-31
Product CodeCGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MICROMEDIC COMBOSTAT LH/FSH KIT is the device name listed in this FDA 510(k) record. The listed applicant is Micromedic Systems. It received FDA 510(k) clearance on 1987-07-31 under 510(k) number K872309. 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 MICROMEDIC COMBOSTAT LH/FSH KIT?

MICROMEDIC COMBOSTAT LH/FSH KIT is a medical device that received FDA 510(k) clearance on 1987-07-31. The listed applicant is Micromedic Systems. The 510(k) number is K872309.

When did MICROMEDIC COMBOSTAT LH/FSH KIT receive FDA 510(k) clearance?

MICROMEDIC COMBOSTAT LH/FSH KIT received FDA 510(k) clearance on 1987-07-31, under 510(k) number K872309.

Who is the listed applicant for MICROMEDIC COMBOSTAT LH/FSH KIT?

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

What is the FDA product code for MICROMEDIC COMBOSTAT LH/FSH KIT?

The FDA product code for MICROMEDIC COMBOSTAT LH/FSH KIT is CGJ.

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Other records listing Micromedic Systems 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.

K923643MEDICOOLK870904MICROMEDIC NEONATAL TSH MONOCLONAL IRMA KITK871505AUTOPAK NEONATAL TSH MONOCLONAL IRMA KITK871008MICROMEDIC NEONATAL T4 KITK870245AUTOPAK TSH MONOCLONAL IRMA KITK862206TAURUS (TM) AUTOMATIC LIQUID SCINTILLATION COUNTER

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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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