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CAVITRON ULTRASONIC SURG. ASPIR. CUSA

Page Type
Cleared 510(K)
510(k) Number
K801623
510(k) Type
Traditional
Applicant
CAVITRON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/1980
Days to Decision
126 days

CAVITRON ULTRASONIC SURG. ASPIR. CUSA

Page Type
Cleared 510(K)
510(k) Number
K801623
510(k) Type
Traditional
Applicant
CAVITRON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/1980
Days to Decision
126 days