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ULTRASOUND GENERATOR MODLE 2270

Page Type
Cleared 510(K)
510(k) Number
K920235
510(k) Type
Traditional
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/1992
Days to Decision
325 days
Submission Type
Statement

ULTRASOUND GENERATOR MODLE 2270

Page Type
Cleared 510(K)
510(k) Number
K920235
510(k) Type
Traditional
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/1992
Days to Decision
325 days
Submission Type
Statement