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FDA 510(k)

SLIT LAMP, H-201

K-Number: K936209 · 1994-04-01

Decision Date1994-04-01
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SLIT LAMP, H-201 is the device name listed in this FDA 510(k) record. The listed applicant is Canon USA, Inc.. It received FDA 510(k) clearance on 1994-04-01 under 510(k) number K936209. 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, 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.

View all 48 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

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