Last synced on 4 February 2023 at 10:33 pm

PORTABLE ACUIOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842567
510(k) Type
Traditional
Applicant
RANDWAL INSTRUMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1984
Days to Decision
44 days

PORTABLE ACUIOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842567
510(k) Type
Traditional
Applicant
RANDWAL INSTRUMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1984
Days to Decision
44 days