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UROTEK LASER CATHETER

Page Type
Cleared 510(K)
510(k) Number
K934389
510(k) Type
Traditional
Applicant
ENERGY LIFE SYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1994
Days to Decision
147 days
Submission Type
Statement

UROTEK LASER CATHETER

Page Type
Cleared 510(K)
510(k) Number
K934389
510(k) Type
Traditional
Applicant
ENERGY LIFE SYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1994
Days to Decision
147 days
Submission Type
Statement