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PIDURAL STEROID SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K945484
510(k) Type
Traditional
Applicant
PROFESSIONAL MEDICAL DEVICE CONSULTANTS
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/2/1995
Days to Decision
206 days
Submission Type
Statement

PIDURAL STEROID SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K945484
510(k) Type
Traditional
Applicant
PROFESSIONAL MEDICAL DEVICE CONSULTANTS
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/2/1995
Days to Decision
206 days
Submission Type
Statement