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PRO-VENT, PULSATOR ARTERIAL BLOOD SAMPLING SYRINGES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981035
510(k) Type
Traditional
Applicant
SIMS PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1998
Days to Decision
33 days
Submission Type
Summary

PRO-VENT, PULSATOR ARTERIAL BLOOD SAMPLING SYRINGES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981035
510(k) Type
Traditional
Applicant
SIMS PORTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1998
Days to Decision
33 days
Submission Type
Summary