Last synced on 14 November 2025 at 11:06 pm

ULTRACISION ULTRASONIC SCALPEL

Page Type
Cleared 510(K)
510(k) Number
K895252
510(k) Type
Traditional
Applicant
ULTRACISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/1989
Days to Decision
71 days

ULTRACISION ULTRASONIC SCALPEL

Page Type
Cleared 510(K)
510(k) Number
K895252
510(k) Type
Traditional
Applicant
ULTRACISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/1989
Days to Decision
71 days