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FDA 510(k)

SLIT LAMP SL-2G

K-Number: K110489 · 2011-05-23

Decision Date2011-05-23
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SLIT LAMP SL-2G is the device name listed in this FDA 510(k) record. The listed applicant is Topcon Medical Systems, Inc.. It received FDA 510(k) clearance on 2011-05-23 under 510(k) number K110489. 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 SLIT LAMP SL-2G?

SLIT LAMP SL-2G is a medical device that received FDA 510(k) clearance on 2011-05-23. The listed applicant is Topcon Medical Systems, Inc.. The 510(k) number is K110489.

When did SLIT LAMP SL-2G receive FDA 510(k) clearance?

SLIT LAMP SL-2G received FDA 510(k) clearance on 2011-05-23, under 510(k) number K110489.

Who is the listed applicant for SLIT LAMP SL-2G?

The FDA 510(k) record lists Topcon Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SLIT LAMP SL-2G?

The FDA product code for SLIT LAMP SL-2G is HJO.

Other records listing Topcon Medical Systems, Inc. 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.

View all 10 devices →

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

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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