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FLEXSURE HP,CONTROLS FOR FLEXSUREHP,FLEXPACK HP(ABBOTT DIAGNOSTICS)ANDCONTROLS FOR FLEXPACK HP (ABBOTT DIAGNOSTICS)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960183
510(k) Type
Traditional
Applicant
Smithkline Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/1996
Days to Decision
143 days
Submission Type
Summary

FLEXSURE HP,CONTROLS FOR FLEXSUREHP,FLEXPACK HP(ABBOTT DIAGNOSTICS)ANDCONTROLS FOR FLEXPACK HP (ABBOTT DIAGNOSTICS)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960183
510(k) Type
Traditional
Applicant
Smithkline Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/1996
Days to Decision
143 days
Submission Type
Summary