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MODIFICATION TO: LOFRIC PLUS SINGLE USE URINARY CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012374
510(k) Type
Special
Applicant
Astra Tech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2001
Days to Decision
28 days
Submission Type
Summary

MODIFICATION TO: LOFRIC PLUS SINGLE USE URINARY CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012374
510(k) Type
Special
Applicant
Astra Tech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2001
Days to Decision
28 days
Submission Type
Summary