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FLEXIFLO LOW-PROFILE BALLOON GASTROSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K962554
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/1997
Days to Decision
494 days
Submission Type
Statement

FLEXIFLO LOW-PROFILE BALLOON GASTROSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K962554
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/1997
Days to Decision
494 days
Submission Type
Statement