Last synced on 14 November 2025 at 11:06 pm

VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER

Page Type
Cleared 510(K)
510(k) Number
K827577
510(k) Type
Traditional
Applicant
RANDWAL INSTRUMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1983
Days to Decision
35 days

VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER

Page Type
Cleared 510(K)
510(k) Number
K827577
510(k) Type
Traditional
Applicant
RANDWAL INSTRUMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1983
Days to Decision
35 days