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LIFERX

Page Type
Cleared 510(K)
510(k) Number
K001596
510(k) Type
Traditional
Applicant
BOWDENGS TECHNOLOGIES, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2000
Days to Decision
44 days
Submission Type
Summary

LIFERX

Page Type
Cleared 510(K)
510(k) Number
K001596
510(k) Type
Traditional
Applicant
BOWDENGS TECHNOLOGIES, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2000
Days to Decision
44 days
Submission Type
Summary