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FDA 510(k)

MINICLINIC OVULATION PREDICTION TEST

K-Number: K910351 · 1991-03-21

ApplicantVanguard Biomedical Corp.
Decision Date1991-03-21
Product CodeCEP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MINICLINIC OVULATION PREDICTION TEST is the device name listed in this FDA 510(k) record. The listed applicant is Vanguard Biomedical Corp.. It received FDA 510(k) clearance on 1991-03-21 under 510(k) number K910351. The device is classified under product code CEP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINICLINIC OVULATION PREDICTION TEST?

MINICLINIC OVULATION PREDICTION TEST is a medical device that received FDA 510(k) clearance on 1991-03-21. The listed applicant is Vanguard Biomedical Corp.. The 510(k) number is K910351.

When did MINICLINIC OVULATION PREDICTION TEST receive FDA 510(k) clearance?

MINICLINIC OVULATION PREDICTION TEST received FDA 510(k) clearance on 1991-03-21, under 510(k) number K910351.

Who is the listed applicant for MINICLINIC OVULATION PREDICTION TEST?

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

What is the FDA product code for MINICLINIC OVULATION PREDICTION TEST?

The FDA product code for MINICLINIC OVULATION PREDICTION TEST is CEP.

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Other records listing Vanguard Biomedical Corp. as applicant

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K960733MINISTICK PREGNANCY TESTK960233MINICLINIC OVULATION PREDICTORK930014PROCLINIC ONE-STEP DIPSTICK PREGNANCY TESTK914254HOMECLINIC ONE STEP PREGNANCY TESTK914253PROCLINIC ONE STEP PREGNANCY TESTK895560MODIFIED HOMECLINIC PREGNANCY TEST

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Related Devices (Code: CEP)

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.

K013582MAYBE?MOM MINI OVULATION MICROSCOPEMaybe?MomK022829INSTANT-VIEW LH OVULATION PREDICTING TESTAlfa Scientific Designs, Inc.K021409AT HOME OVULATION TEST, MODEL 9032Phamatech, Inc.K013874CLEARPLANE EASY OVULATION TESTUnipath , Ltd.K013323TCI-31 LIFELONG OVULATION TESTERTci New YorkK012252QUIK-CHECK OVULATION PREDICTORACON Laboratories, 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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