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FDA 510(k)

Barricaid Instrument Tray

K-Number: K201676 · 2020-07-16

ApplicantIntrinsic Therapeutics, Inc.
Decision Date2020-07-16
Product CodeQHG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Barricaid Instrument Tray is a medical device manufactured by Intrinsic Therapeutics, Inc.. It received FDA 510(k) clearance on 2020-07-16 under approval number K201676. The device is classified under product code QHG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Barricaid Instrument Tray?

Barricaid Instrument Tray is a medical device that received FDA 510(k) clearance on 2020-07-16. It is manufactured by Intrinsic Therapeutics, Inc.. The 510(k) number is K201676.

When was Barricaid Instrument Tray approved by the FDA?

Barricaid Instrument Tray received FDA 510(k) clearance on 2020-07-16, under approval number K201676.

What company makes Barricaid Instrument Tray?

Barricaid Instrument Tray is manufactured by Intrinsic Therapeutics, Inc..

What is the FDA product code for Barricaid Instrument Tray?

The FDA product code for Barricaid Instrument Tray is QHG.

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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