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GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES

Page Type
Cleared 510(K)
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)
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