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INFANT REFLUX SLING

Page Type
Cleared 510(K)
510(k) Number
K905630
510(k) Type
Traditional
Applicant
PEDICRAFT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1991
Days to Decision
89 days

INFANT REFLUX SLING

Page Type
Cleared 510(K)
510(k) Number
K905630
510(k) Type
Traditional
Applicant
PEDICRAFT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1991
Days to Decision
89 days