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FOG CONTROL, LENS FOG REDUCTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K932300
510(k) Type
Traditional
Applicant
HIGHPOINT MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1993
Days to Decision
128 days
Submission Type
Statement

FOG CONTROL, LENS FOG REDUCTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K932300
510(k) Type
Traditional
Applicant
HIGHPOINT MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1993
Days to Decision
128 days
Submission Type
Statement