Last synced on 13 June 2025 at 11:06 pm

SYNERMED LDH REAGENT KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903773
510(k) Type
Traditional
Applicant
SYNERMED, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
10/12/1990
Days to Decision
53 days

SYNERMED LDH REAGENT KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903773
510(k) Type
Traditional
Applicant
SYNERMED, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
10/12/1990
Days to Decision
53 days