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FDA 510(k)

SLIT LAMP

K-Number: K073190 · 2008-01-11

Decision Date2008-01-11
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SLIT LAMP is the device name listed in this FDA 510(k) record. The listed applicant is Huvitz Co., Ltd.. It received FDA 510(k) clearance on 2008-01-11 under 510(k) number K073190. 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?

SLIT LAMP is a medical device that received FDA 510(k) clearance on 2008-01-11. The listed applicant is Huvitz Co., Ltd.. The 510(k) number is K073190.

When did SLIT LAMP receive FDA 510(k) clearance?

SLIT LAMP received FDA 510(k) clearance on 2008-01-11, under 510(k) number K073190.

Who is the listed applicant for SLIT LAMP?

The FDA 510(k) record lists Huvitz Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SLIT LAMP?

The FDA product code for SLIT LAMP is HJO.

Other records listing Huvitz Co., Ltd. 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.

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.

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