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FDA 510(k)

SL 220

K-Number: K162684 · 2017-05-31

Decision Date2017-05-31
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SL 220 is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss Meditec, AG. It received FDA 510(k) clearance on 2017-05-31 under 510(k) 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. The listed applicant is Carl Zeiss Meditec, AG. The 510(k) number is K162684.

When did SL 220 receive FDA 510(k) clearance?

SL 220 received FDA 510(k) clearance on 2017-05-31, under 510(k) number K162684.

Who is the listed applicant for SL 220?

The FDA 510(k) record lists Carl Zeiss Meditec, AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SL 220?

The FDA product code for SL 220 is HJO.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Carl Zeiss Meditec, AG as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: HJO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.