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MODIFIED DECANNULATION STOPPER

Page Type
Cleared 510(K)
510(k) Number
K894050
510(k) Type
Traditional
Applicant
PREMIER MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1989
Days to Decision
55 days

MODIFIED DECANNULATION STOPPER

Page Type
Cleared 510(K)
510(k) Number
K894050
510(k) Type
Traditional
Applicant
PREMIER MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1989
Days to Decision
55 days