Atlas FDA

SLIT LAMP

FDA 510(k) clearance K073190 · decided 2008-01-11

Clearance details

K-number
K073190
Device name
SLIT LAMP
Applicant
Huvitz Co., Ltd.
Decision
Substantially Equivalent
Date received
2007-11-13
Decision date
2008-01-11
Days to decision
59 days
Clearance type
Traditional
Product code
HJO
Device class
2
Regulation number
886.1850
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Flintville, TN, US
Third-party review
Yes
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.