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FDA 510(k)

UNILET LANCET

K-Number: K842517 · 1984-09-20

ApplicantUlster Scientific, Inc.
Decision Date1984-09-20
Product CodeFML
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UNILET LANCET is the device name listed in this FDA 510(k) record. The listed applicant is Ulster Scientific, Inc.. It received FDA 510(k) clearance on 1984-09-20 under 510(k) number K842517. The device is classified under product code FML. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNILET LANCET?

UNILET LANCET is a medical device that received FDA 510(k) clearance on 1984-09-20. The listed applicant is Ulster Scientific, Inc.. The 510(k) number is K842517.

When did UNILET LANCET receive FDA 510(k) clearance?

UNILET LANCET received FDA 510(k) clearance on 1984-09-20, under 510(k) number K842517.

Who is the listed applicant for UNILET LANCET?

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

What is the FDA product code for UNILET LANCET?

The FDA product code for UNILET LANCET is FML.

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Other records listing Ulster Scientific, Inc. as applicant

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Related Devices (Code: FML)

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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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