Last synced on 25 November 2022 at 11:04 pm

MEDISYSTEMS PHERESIS NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862002
510(k) Type
Traditional
Applicant
MEDISYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1986
Days to Decision
35 days

MEDISYSTEMS PHERESIS NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862002
510(k) Type
Traditional
Applicant
MEDISYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1986
Days to Decision
35 days