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PLEXUS/3000 (P/3000), PLEXUS/3500 (P/3500)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952610
510(k) Type
Traditional
Applicant
PLEXUS MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1995
Days to Decision
98 days
Submission Type
Statement

PLEXUS/3000 (P/3000), PLEXUS/3500 (P/3500)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952610
510(k) Type
Traditional
Applicant
PLEXUS MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1995
Days to Decision
98 days
Submission Type
Statement