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QUANTEX RF PLUS (LATEX, BUFFER STANDARD, CONTROL)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896271
510(k) Type
Traditional
Applicant
BIOKIT USA, INC.
Country
Spain
FDA Decision
Substantially Equivalent
Decision Date
11/8/1989
Days to Decision
9 days

QUANTEX RF PLUS (LATEX, BUFFER STANDARD, CONTROL)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896271
510(k) Type
Traditional
Applicant
BIOKIT USA, INC.
Country
Spain
FDA Decision
Substantially Equivalent
Decision Date
11/8/1989
Days to Decision
9 days