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AESKULISA MPO, MODEL 30-7303US

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091860
510(k) Type
Traditional
Applicant
AESKU.DIAGNOSTICS
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/23/2010
Days to Decision
249 days
Submission Type
Statement

AESKULISA MPO, MODEL 30-7303US

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091860
510(k) Type
Traditional
Applicant
AESKU.DIAGNOSTICS
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/23/2010
Days to Decision
249 days
Submission Type
Statement