Last synced on 14 November 2025 at 11:06 pm

B-HCG

Page Type
Cleared 510(K)
510(k) Number
K822343
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1982
Days to Decision
28 days

B-HCG

Page Type
Cleared 510(K)
510(k) Number
K822343
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1982
Days to Decision
28 days