Last synced on 16 May 2025 at 11:05 pm

MODIFIED LABEL FOR EMBRIA-CK, QUICK-MB/MICROMI-MB

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901450
510(k) Type
Traditional
Applicant
INTL. IMMUNOASSAY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/1990
Days to Decision
48 days

MODIFIED LABEL FOR EMBRIA-CK, QUICK-MB/MICROMI-MB

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901450
510(k) Type
Traditional
Applicant
INTL. IMMUNOASSAY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/1990
Days to Decision
48 days