Last synced on 11 July 2025 at 11:06 pm

TUMARK PROFESSIONAL, MODEL 271560; MR- TUMARK PROFESSIONAL, MODEL 601560

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073095
510(k) Type
Traditional
Applicant
SOMATEX MEDICAL TECHNOLOGIES GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2008
Days to Decision
139 days
Submission Type
Summary

TUMARK PROFESSIONAL, MODEL 271560; MR- TUMARK PROFESSIONAL, MODEL 601560

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073095
510(k) Type
Traditional
Applicant
SOMATEX MEDICAL TECHNOLOGIES GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2008
Days to Decision
139 days
Submission Type
Summary