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FDA 510(k)

NANCY NAIL

K-Number: K960642 · 1996-05-17

ApplicantLandos, Inc.
Decision Date1996-05-17
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NANCY NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Landos, Inc.. It received FDA 510(k) clearance on 1996-05-17 under 510(k) number K960642. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NANCY NAIL?

NANCY NAIL is a medical device that received FDA 510(k) clearance on 1996-05-17. The listed applicant is Landos, Inc.. The 510(k) number is K960642.

When did NANCY NAIL receive FDA 510(k) clearance?

NANCY NAIL received FDA 510(k) clearance on 1996-05-17, under 510(k) number K960642.

Who is the listed applicant for NANCY NAIL?

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

What is the FDA product code for NANCY NAIL?

The FDA product code for NANCY NAIL is HTY.

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Other records listing Landos, Inc. as applicant

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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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