SLIT LAMP, H-201
K-Number: K936209 · 1994-04-01
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Device Summary
Frequently Asked Questions
What is the SLIT LAMP, H-201?
SLIT LAMP, H-201 is a medical device that received FDA 510(k) clearance on 1994-04-01. The listed applicant is Canon USA, Inc.. The 510(k) number is K936209.
When did SLIT LAMP, H-201 receive FDA 510(k) clearance?
SLIT LAMP, H-201 received FDA 510(k) clearance on 1994-04-01, under 510(k) number K936209.
Who is the listed applicant for SLIT LAMP, H-201?
The FDA 510(k) record lists Canon USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SLIT LAMP, H-201?
The FDA product code for SLIT LAMP, H-201 is HJO.
Other records listing Canon USA, 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.
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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