Last synced on 27 January 2023 at 11:04 pm

RE-USABLE BIPOLAR CONCENTRIC NEEDLE(237-XXX-24,237-XXX-24STP, 237-XXX-24TP,237-XXX-24STP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960591
510(k) Type
Traditional
Applicant
CHALGREN ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/1996
Days to Decision
122 days
Submission Type
Statement

RE-USABLE BIPOLAR CONCENTRIC NEEDLE(237-XXX-24,237-XXX-24STP, 237-XXX-24TP,237-XXX-24STP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960591
510(k) Type
Traditional
Applicant
CHALGREN ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/1996
Days to Decision
122 days
Submission Type
Statement