Last synced on 10 January 2025 at 11:05 pm

UNIVERSAL PLUS ES S/I INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954056
510(k) Type
Traditional
Applicant
CONMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1995
Days to Decision
31 days
Submission Type
Statement

UNIVERSAL PLUS ES S/I INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954056
510(k) Type
Traditional
Applicant
CONMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1995
Days to Decision
31 days
Submission Type
Statement