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J & J I-330 SERIES PHYSIOLOGICAL MONITORING & BIOFEEDBACK INSTUMENT AND USE SOFTWARE APPLICATIONS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K945826
510(k) Type
Traditional
Applicant
MEDICAL DEVICE INSPECTION CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1995
Days to Decision
248 days
Submission Type
Statement

J & J I-330 SERIES PHYSIOLOGICAL MONITORING & BIOFEEDBACK INSTUMENT AND USE SOFTWARE APPLICATIONS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K945826
510(k) Type
Traditional
Applicant
MEDICAL DEVICE INSPECTION CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1995
Days to Decision
248 days
Submission Type
Statement