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FDA 510(k)

VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles

K-Number: K170070 · 2017-04-28

ApplicantSTERIS Corporation
Decision Date2017-04-28
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2017-04-28 under 510(k) number K170070. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles?

VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles is a medical device that received FDA 510(k) clearance on 2017-04-28. The listed applicant is STERIS Corporation. The 510(k) number is K170070.

When did VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles receive FDA 510(k) clearance?

VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles received FDA 510(k) clearance on 2017-04-28, under 510(k) number K170070.

Who is the listed applicant for VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles?

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 VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles?

The FDA product code for VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles is FRC.

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Related Devices (Code: FRC)

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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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