Last synced on 31 March 2023 at 11:04 pm

SYNERMED PHOSPHORUS REAGENT KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912569
510(k) Type
Traditional
Applicant
SYNERMED, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
7/17/1991
Days to Decision
36 days
Submission Type
Statement

SYNERMED PHOSPHORUS REAGENT KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912569
510(k) Type
Traditional
Applicant
SYNERMED, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
7/17/1991
Days to Decision
36 days
Submission Type
Statement