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FDA 510(k)

GYRUS ACMI TELESCOPE STORAGE-STERILIZATION TRAY

K-Number: K120474 · 2012-07-10

ApplicantGyrus Acmi, Inc.
Decision Date2012-07-10
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GYRUS ACMI TELESCOPE STORAGE-STERILIZATION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Gyrus Acmi, Inc.. It received FDA 510(k) clearance on 2012-07-10 under 510(k) number K120474. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GYRUS ACMI TELESCOPE STORAGE-STERILIZATION TRAY?

GYRUS ACMI TELESCOPE STORAGE-STERILIZATION TRAY is a medical device that received FDA 510(k) clearance on 2012-07-10. The listed applicant is Gyrus Acmi, Inc.. The 510(k) number is K120474.

When did GYRUS ACMI TELESCOPE STORAGE-STERILIZATION TRAY receive FDA 510(k) clearance?

GYRUS ACMI TELESCOPE STORAGE-STERILIZATION TRAY received FDA 510(k) clearance on 2012-07-10, under 510(k) number K120474.

Who is the listed applicant for GYRUS ACMI TELESCOPE STORAGE-STERILIZATION TRAY?

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

What is the FDA product code for GYRUS ACMI TELESCOPE STORAGE-STERILIZATION TRAY?

The FDA product code for GYRUS ACMI TELESCOPE STORAGE-STERILIZATION TRAY is KCT.

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Related Devices (Code: KCT)

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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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