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BIO NUCLEAR DIAGNOSTICS (ENDO)CERVICAL SAMPLER FOR GYN CYTOLOGY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081522
510(k) Type
Traditional
Applicant
BIO NUCLEAR DIAGNOSTICS, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
12/5/2008
Days to Decision
189 days
Submission Type
Statement

BIO NUCLEAR DIAGNOSTICS (ENDO)CERVICAL SAMPLER FOR GYN CYTOLOGY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081522
510(k) Type
Traditional
Applicant
BIO NUCLEAR DIAGNOSTICS, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
12/5/2008
Days to Decision
189 days
Submission Type
Statement