Last synced on 9 May 2025 at 11:05 pm

RATEMINDER(TM) V INFUSION PUMP, MODIFICATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911769
510(k) Type
Traditional
Applicant
CRITIKON COMPANY,LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/1991
Days to Decision
45 days
Submission Type
Statement

RATEMINDER(TM) V INFUSION PUMP, MODIFICATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911769
510(k) Type
Traditional
Applicant
CRITIKON COMPANY,LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/1991
Days to Decision
45 days
Submission Type
Statement