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ACCESSORY TO EYEDROP GUIDE

Page Type
Cleared 510(K)
510(k) Number
K884974
510(k) Type
Traditional
Applicant
SUREDROP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1989
Days to Decision
114 days

ACCESSORY TO EYEDROP GUIDE

Page Type
Cleared 510(K)
510(k) Number
K884974
510(k) Type
Traditional
Applicant
SUREDROP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1989
Days to Decision
114 days