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ORION'S URETHRAL CATHETERIZATION KIT WITH CATHETER AND BAG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944378
510(k) Type
Traditional
Applicant
REGULATORY & MARKETING SERVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/1995
Days to Decision
161 days
Submission Type
Statement

ORION'S URETHRAL CATHETERIZATION KIT WITH CATHETER AND BAG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944378
510(k) Type
Traditional
Applicant
REGULATORY & MARKETING SERVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/1995
Days to Decision
161 days
Submission Type
Statement