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 a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2017-04-28 under approval 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. It is manufactured by STERIS Corporation. The 510(k) number is K170070.
When was VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles approved by the FDA?
VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles received FDA 510(k) clearance on 2017-04-28, under approval number K170070.
What company makes VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles?
VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles is manufactured by STERIS Corporation.
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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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.