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MAXI-FLOW

Page Type
Cleared 510(K)
510(k) Number
K955150
510(k) Type
Traditional
Applicant
Bio-Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/1996
Days to Decision
71 days
Submission Type
Statement

MAXI-FLOW

Page Type
Cleared 510(K)
510(k) Number
K955150
510(k) Type
Traditional
Applicant
Bio-Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/1996
Days to Decision
71 days
Submission Type
Statement