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FDA 510(k)

VHP 136 TRAY

K-Number: K070769 · 2007-10-05

ApplicantSTERIS Corporation
Decision Date2007-10-05
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VHP 136 TRAY is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2007-10-05 under 510(k) number K070769. 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 VHP 136 TRAY?

VHP 136 TRAY is a medical device that received FDA 510(k) clearance on 2007-10-05. The listed applicant is STERIS Corporation. The 510(k) number is K070769.

When did VHP 136 TRAY receive FDA 510(k) clearance?

VHP 136 TRAY received FDA 510(k) clearance on 2007-10-05, under 510(k) number K070769.

Who is the listed applicant for VHP 136 TRAY?

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

What is the FDA product code for VHP 136 TRAY?

The FDA product code for VHP 136 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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