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GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972158
510(k) Type
Traditional
Applicant
PRINCETON REGULATORY ASSOC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/1998
Days to Decision
256 days
Submission Type
Statement

GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972158
510(k) Type
Traditional
Applicant
PRINCETON REGULATORY ASSOC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/1998
Days to Decision
256 days
Submission Type
Statement