Last synced on 14 November 2025 at 11:06 pm

COAGULATING CANNULA DEVICE

Page Type
Cleared 510(K)
510(k) Number
K953696
510(k) Type
Traditional
Applicant
DORSAL ORTHOPEDIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/1995
Days to Decision
122 days
Submission Type
Statement

COAGULATING CANNULA DEVICE

Page Type
Cleared 510(K)
510(k) Number
K953696
510(k) Type
Traditional
Applicant
DORSAL ORTHOPEDIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/1995
Days to Decision
122 days
Submission Type
Statement