Last synced on 30 September 2022 at 11:05 pm

PIDURAL STEROID SYSTEM

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