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ULTRACISON HARMONIC SCALPEL HS2 BLADE

Page Type
Cleared 510(K)
510(k) Number
K941897
510(k) Type
Traditional
Applicant
ULTRACISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1994
Days to Decision
74 days
Submission Type
Statement

ULTRACISON HARMONIC SCALPEL HS2 BLADE

Page Type
Cleared 510(K)
510(k) Number
K941897
510(k) Type
Traditional
Applicant
ULTRACISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1994
Days to Decision
74 days
Submission Type
Statement