Last synced on 23 September 2022 at 11:05 pm

LDH REAGENT SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812836
510(k) Type
Traditional
Applicant
ANCO MEDICAL REAGENTS & ASSOC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
10/9/1981
Days to Decision
0 days

LDH REAGENT SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812836
510(k) Type
Traditional
Applicant
ANCO MEDICAL REAGENTS & ASSOC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
10/9/1981
Days to Decision
0 days