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FDA 510(k)

VIS-DISK HCG (EIA) JPL-041M

K-Number: K891096 · 1989-06-16

ApplicantLeeco Diagnostics, Inc.
Decision Date1989-06-16
Product CodeDHA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VIS-DISK HCG (EIA) JPL-041M 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 1989-06-16 under 510(k) number K891096. The device is classified under product code DHA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIS-DISK HCG (EIA) JPL-041M?

VIS-DISK HCG (EIA) JPL-041M is a medical device that received FDA 510(k) clearance on 1989-06-16. The listed applicant is Leeco Diagnostics, Inc.. The 510(k) number is K891096.

When did VIS-DISK HCG (EIA) JPL-041M receive FDA 510(k) clearance?

VIS-DISK HCG (EIA) JPL-041M received FDA 510(k) clearance on 1989-06-16, under 510(k) number K891096.

Who is the listed applicant for VIS-DISK HCG (EIA) JPL-041M?

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 VIS-DISK HCG (EIA) JPL-041M?

The FDA product code for VIS-DISK HCG (EIA) JPL-041M is DHA.

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-044MK883269PRL-QUANTK880577CONCEP-7-BHCGK880069LEECO PREGNASTICK (EIA) CATALOG #003

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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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