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FLEXIFLO STOMATE DECOMPRESSION TUBE

Page Type
Cleared 510(K)
510(k) Number
K903579
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1990
Days to Decision
111 days

FLEXIFLO STOMATE DECOMPRESSION TUBE

Page Type
Cleared 510(K)
510(k) Number
K903579
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1990
Days to Decision
111 days