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FRITCH OPHTHALMIC ENDOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K855151
510(k) Type
Traditional
Applicant
REGTEC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1986
Days to Decision
55 days

FRITCH OPHTHALMIC ENDOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K855151
510(k) Type
Traditional
Applicant
REGTEC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1986
Days to Decision
55 days