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FDA 510(k)

DIAGNOSTIC KIT, FERRITAB-FE-59

K-Number: K782159 · 1979-02-01

ApplicantLeeco Diagnostics, Inc.
Decision Date1979-02-01
Product CodeJJA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIAGNOSTIC KIT, FERRITAB-FE-59 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 1979-02-01 under 510(k) number K782159. The device is classified under product code JJA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAGNOSTIC KIT, FERRITAB-FE-59?

DIAGNOSTIC KIT, FERRITAB-FE-59 is a medical device that received FDA 510(k) clearance on 1979-02-01. The listed applicant is Leeco Diagnostics, Inc.. The 510(k) number is K782159.

When did DIAGNOSTIC KIT, FERRITAB-FE-59 receive FDA 510(k) clearance?

DIAGNOSTIC KIT, FERRITAB-FE-59 received FDA 510(k) clearance on 1979-02-01, under 510(k) number K782159.

Who is the listed applicant for DIAGNOSTIC KIT, FERRITAB-FE-59?

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 DIAGNOSTIC KIT, FERRITAB-FE-59?

The FDA product code for DIAGNOSTIC KIT, FERRITAB-FE-59 is JJA.

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Other records listing Leeco Diagnostics, Inc. as applicant

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Related Devices (Code: JJA)

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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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