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FDA 510(k)

NAIL SPLINT

K-Number: K850803 · 1985-10-16

ApplicantInro Medical Designs, Inc.
Decision Date1985-10-16
Product CodeMQZ
DecisionSubstantially Equivalent

Device Summary

NAIL SPLINT is the device name listed in this FDA 510(k) record. The listed applicant is Inro Medical Designs, Inc.. It received FDA 510(k) clearance on 1985-10-16 under 510(k) number K850803. The device is classified under product code MQZ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAIL SPLINT?

NAIL SPLINT is a medical device that received FDA 510(k) clearance on 1985-10-16. The listed applicant is Inro Medical Designs, Inc.. The 510(k) number is K850803.

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

NAIL SPLINT received FDA 510(k) clearance on 1985-10-16, under 510(k) number K850803.

Who is the listed applicant for NAIL SPLINT?

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

What is the FDA product code for NAIL SPLINT?

The FDA product code for NAIL SPLINT is MQZ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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