SL 220
K-Number: K162684 · 2017-05-31
ApplicantCarl Zeiss Meditec, AG
Decision Date2017-05-31
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
SL 220 is a medical device manufactured by Carl Zeiss Meditec, AG. It received FDA 510(k) clearance on 2017-05-31 under approval number K162684. The device is classified under product code HJO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SL 220?
SL 220 is a medical device that received FDA 510(k) clearance on 2017-05-31. It is manufactured by Carl Zeiss Meditec, AG. The 510(k) number is K162684.
When was SL 220 approved by the FDA?
SL 220 received FDA 510(k) clearance on 2017-05-31, under approval number K162684.
What company makes SL 220?
SL 220 is manufactured by Carl Zeiss Meditec, AG.
What is the FDA product code for SL 220?
The FDA product code for SL 220 is HJO.
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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.