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ULTRAPAC II SX PLUS (TM)

Page Type
Cleared 510(K)
510(k) Number
K872657
510(k) Type
Traditional
Applicant
MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1987
Days to Decision
28 days

ULTRAPAC II SX PLUS (TM)

Page Type
Cleared 510(K)
510(k) Number
K872657
510(k) Type
Traditional
Applicant
MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1987
Days to Decision
28 days