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NOCTURNAL PENILE TUMESCENCE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K870983
510(k) Type
Traditional
Applicant
TEXAS MEDICAL ELECTRONICS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1987
Days to Decision
105 days

NOCTURNAL PENILE TUMESCENCE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K870983
510(k) Type
Traditional
Applicant
TEXAS MEDICAL ELECTRONICS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1987
Days to Decision
105 days