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AVISO OPHTHALMIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K051851
510(k) Type
Special
Applicant
QUANTEL MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2005
Days to Decision
26 days
Submission Type
Summary

AVISO OPHTHALMIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K051851
510(k) Type
Special
Applicant
QUANTEL MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2005
Days to Decision
26 days
Submission Type
Summary