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DENLEY ANTHOS 2001 READER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894270
510(k) Type
Traditional
Applicant
DENLEY INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1989
Days to Decision
60 days

DENLEY ANTHOS 2001 READER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894270
510(k) Type
Traditional
Applicant
DENLEY INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1989
Days to Decision
60 days