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MODIFIED SLIDING RECONSTITUTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K884626
510(k) Type
Traditional
Applicant
BAXTER HEALTHCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1988
Days to Decision
15 days

MODIFIED SLIDING RECONSTITUTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K884626
510(k) Type
Traditional
Applicant
BAXTER HEALTHCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1988
Days to Decision
15 days