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FDA 510(k)

CLEARPLAN EASY

K-Number: K894579 · 1989-10-12

ApplicantUnipath , Ltd.
Decision Date1989-10-12
Product CodeCEP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CLEARPLAN EASY is the device name listed in this FDA 510(k) record. The listed applicant is Unipath , Ltd.. It received FDA 510(k) clearance on 1989-10-12 under 510(k) number K894579. 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 CLEARPLAN EASY?

CLEARPLAN EASY is a medical device that received FDA 510(k) clearance on 1989-10-12. The listed applicant is Unipath , Ltd.. The 510(k) number is K894579.

When did CLEARPLAN EASY receive FDA 510(k) clearance?

CLEARPLAN EASY received FDA 510(k) clearance on 1989-10-12, under 510(k) number K894579.

Who is the listed applicant for CLEARPLAN EASY?

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

What is the FDA product code for CLEARPLAN EASY?

The FDA product code for CLEARPLAN EASY is CEP.

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Other records listing Unipath , Ltd. 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.

K061769E.P.T. CERTAINTY 1-STEP PREGNANCY TESTK060128CLEARBLUE EASY DIGITAL PREGNANCY TESTK051638INVERNESS MEDICAL TESTPACK + PLUS STREP A WITH OBCK050930E.P.T. CERTAINTY PREGNANCY TESTK042280FACT PLUS ONE-STEP PREGNANCY TEST KITK041404CLEARBLUE EASY EASY READ 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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