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MODIFIED REFLUX REDUCER

Page Type
Cleared 510(K)
510(k) Number
K883818
510(k) Type
Traditional
Applicant
PHYSICIAN ENGINEERED PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1988
Days to Decision
74 days

MODIFIED REFLUX REDUCER

Page Type
Cleared 510(K)
510(k) Number
K883818
510(k) Type
Traditional
Applicant
PHYSICIAN ENGINEERED PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1988
Days to Decision
74 days