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FLEXIMARC, MODEL CM-0.9-2-10-GG-L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100267
510(k) Type
Traditional
Applicant
CORTEX MANUFACTURING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2010
Days to Decision
26 days
Submission Type
Summary

FLEXIMARC, MODEL CM-0.9-2-10-GG-L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100267
510(k) Type
Traditional
Applicant
CORTEX MANUFACTURING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2010
Days to Decision
26 days
Submission Type
Summary