Last synced on 21 June 2024 at 11:04 pm

SYNERGY PLUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960762
510(k) Type
Traditional
Applicant
THE PROMETHEUS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/1996
Days to Decision
108 days
Submission Type
Statement

SYNERGY PLUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960762
510(k) Type
Traditional
Applicant
THE PROMETHEUS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/1996
Days to Decision
108 days
Submission Type
Statement