Last synced on 25 January 2026 at 3:41 am

K/K (ASMA/ANA) UNIVERSAL BIOPAK

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802299
510(k) Type
Traditional
Applicant
BIOWARE PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1981
Days to Decision
132 days

K/K (ASMA/ANA) UNIVERSAL BIOPAK

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802299
510(k) Type
Traditional
Applicant
BIOWARE PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1981
Days to Decision
132 days