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FDA 510(k)

LEECO PREGNASTICK (EIA) CATALOG #003

K-Number: K880069 · 1988-02-11

ApplicantLeeco Diagnostics, Inc.
Decision Date1988-02-11
Product CodeLCX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LEECO PREGNASTICK (EIA) CATALOG #003 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 1988-02-11 under 510(k) number K880069. The device is classified under product code LCX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEECO PREGNASTICK (EIA) CATALOG #003?

LEECO PREGNASTICK (EIA) CATALOG #003 is a medical device that received FDA 510(k) clearance on 1988-02-11. The listed applicant is Leeco Diagnostics, Inc.. The 510(k) number is K880069.

When did LEECO PREGNASTICK (EIA) CATALOG #003 receive FDA 510(k) clearance?

LEECO PREGNASTICK (EIA) CATALOG #003 received FDA 510(k) clearance on 1988-02-11, under 510(k) number K880069.

Who is the listed applicant for LEECO PREGNASTICK (EIA) CATALOG #003?

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 LEECO PREGNASTICK (EIA) CATALOG #003?

The FDA product code for LEECO PREGNASTICK (EIA) CATALOG #003 is LCX.

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Other records listing Leeco Diagnostics, Inc. as applicant

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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

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Related Devices (Code: LCX)

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.

K251040MissLan® Early Detection Digital Pregnancy Test; MissLan® Early Result Digital Pregnancy TestGuangzhou Decheng Biotechnology Co., Ltd.K251053Shinetell PlusTM Digital Early Pregnancy TestHangzhou AllTest Biotech Co., Ltd.K250117FaStep Pregnancy Rapid Test Cassette; Fastep HCG Rapid Test CassetteAssure Tech., LLCK242135Synthgene Home Test HCG Test Strip; Synthgene Home Test HCG Test Cassette; Synthgene Home Test HCG Test MidstreamNanjing Synthgene Medical Technology Co., Ltd.K243573FaStep Early Pregnancy Rapid Test Strip; FaStep Early Pregnancy Rapid Test Cassette; FaStep Early Pregnancy Rapid Test MidstreamAssure Tech., LLCK241394iHealth® Early Pregnancy Test; iHealth® Early Pregnancy Test StripAndon Health Co, Ltd.

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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