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ACHELASIA BALLOON DIALATOR

Page Type
Cleared 510(K)
510(k) Number
K884715
510(k) Type
Traditional
Applicant
PRIMROSE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1989
Days to Decision
325 days

ACHELASIA BALLOON DIALATOR

Page Type
Cleared 510(K)
510(k) Number
K884715
510(k) Type
Traditional
Applicant
PRIMROSE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1989
Days to Decision
325 days