Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LEE-BEAD BETA LH (EIA)

K-Number: K854838 · 1986-01-07

ApplicantLeeco Diagnostics, Inc.
Decision Date1986-01-07
Product CodeCEP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LEE-BEAD BETA LH (EIA) is the device name listed in this FDA 510(k) record. The listed applicant is Leeco Diagnostics, Inc.. It received FDA 510(k) clearance on 1986-01-07 under 510(k) number K854838. 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 LEE-BEAD BETA LH (EIA)?

LEE-BEAD BETA LH (EIA) is a medical device that received FDA 510(k) clearance on 1986-01-07. The listed applicant is Leeco Diagnostics, Inc.. The 510(k) number is K854838.

When did LEE-BEAD BETA LH (EIA) receive FDA 510(k) clearance?

LEE-BEAD BETA LH (EIA) received FDA 510(k) clearance on 1986-01-07, under 510(k) number K854838.

Who is the listed applicant for LEE-BEAD BETA LH (EIA)?

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

What is the FDA product code for LEE-BEAD BETA LH (EIA)?

The FDA product code for LEE-BEAD BETA LH (EIA) is CEP.

Other records listing Leeco Diagnostics, Inc. 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.

K895765LEECO PREVIEW(R) EBV (EIA)K894122LEECO VIS-DISK STREP-A (EIA)K891095VIS-DISK HCG (EIA) LYOPHILIZED JPL-044MK891096VIS-DISK HCG (EIA) JPL-041MK883269PRL-QUANTK880577CONCEP-7-BHCG

View all 49 devices →

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.

↑