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PRESSURE SORE MANAGEMENT KIT

Page Type
Cleared 510(K)
510(k) Number
K912116
510(k) Type
Traditional
Applicant
MEDICAL DEVICE INSPECTION CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1991
Days to Decision
157 days
Submission Type
Statement

PRESSURE SORE MANAGEMENT KIT

Page Type
Cleared 510(K)
510(k) Number
K912116
510(k) Type
Traditional
Applicant
MEDICAL DEVICE INSPECTION CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1991
Days to Decision
157 days
Submission Type
Statement