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PTI HEART-LIFT(TM) CARDIAC RETRACTION GLOVES-STERI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882381
510(k) Type
Traditional
Applicant
PIONEERING TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/1988
Days to Decision
28 days

PTI HEART-LIFT(TM) CARDIAC RETRACTION GLOVES-STERI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882381
510(k) Type
Traditional
Applicant
PIONEERING TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/1988
Days to Decision
28 days