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ADD'L CLAIMED INTENDED USE FOR IDEIA(TM) CHLAMYDIA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901972
510(k) Type
Traditional
Applicant
NOVO NORDISK DIAGNOSTICS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/5/1990
Days to Decision
127 days

ADD'L CLAIMED INTENDED USE FOR IDEIA(TM) CHLAMYDIA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901972
510(k) Type
Traditional
Applicant
NOVO NORDISK DIAGNOSTICS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/5/1990
Days to Decision
127 days