Last synced on 20 December 2024 at 11:05 pm

LIFERX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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