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ENTEROCLYSIS TUBE

Page Type
Cleared 510(K)
510(k) Number
K923002
510(k) Type
Traditional
Applicant
BIOSEARCH MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/28/1994
Days to Decision
736 days
Submission Type
Statement

ENTEROCLYSIS TUBE

Page Type
Cleared 510(K)
510(k) Number
K923002
510(k) Type
Traditional
Applicant
BIOSEARCH MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/28/1994
Days to Decision
736 days
Submission Type
Statement