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FDA 510(k)

AUTOFLUOR V

K-Number: K861978 · 1986-06-10

ApplicantTechnia Diagnostics , Ltd.
Decision Date1986-06-10
Product CodeKTL
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

AUTOFLUOR V is the device name listed in this FDA 510(k) record. The listed applicant is Technia Diagnostics , Ltd.. It received FDA 510(k) clearance on 1986-06-10 under 510(k) number K861978. The device is classified under product code KTL. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOFLUOR V?

AUTOFLUOR V is a medical device that received FDA 510(k) clearance on 1986-06-10. The listed applicant is Technia Diagnostics , Ltd.. The 510(k) number is K861978.

When did AUTOFLUOR V receive FDA 510(k) clearance?

AUTOFLUOR V received FDA 510(k) clearance on 1986-06-10, under 510(k) number K861978.

Who is the listed applicant for AUTOFLUOR V?

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

What is the FDA product code for AUTOFLUOR V?

The FDA product code for AUTOFLUOR V is KTL.

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Other records listing Technia Diagnostics , Ltd. as applicant

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Related Devices (Code: KTL)

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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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