Atlas FDA

NEVA SYSTEM

FDA 510(k) clearance K980627 · decided 1998-04-07

Clearance details

K-number
K980627
Device name
NEVA SYSTEM
Applicant
Urometrics, Inc.
Decision
Substantially Equivalent
Date received
1998-02-18
Decision date
1998-04-07
Days to decision
48 days
Clearance type
Traditional
Product code
LIL
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
St. Paul, MN, US
Third-party review
No
Expedited review
No

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RecordFirmDate
RIGIDOMETER, MODEL DIR-4U (K061676)Uroan 212006-12-27
PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM) (K062042)Plethora Solutions2006-09-06
PREFTEST PROFESSIONAL SUITE (K052929)Limestone Technologies, Inc.2006-04-26
MONARCH 21 PENILE PLETHYSMOGRAPH SYSTEM (K033126)Behavioral Technology, Inc.2003-10-29
DIGITAL INFLECTION RIGIDOMETER (DIR) (K000194)Uroan Xxi Electromedicina2000-04-10
VISER PENILE TUMESCENCE MONITOR (K991479)Laborie Medical Tech Corp.1999-07-07
CAT-600 PENILE PLETHYSMOGRAPH (K936115)Farrall Instruments, Inc.1995-01-10
CAT-400UL PENILE PLETHYSMOGRAPH (K940128)Farrall Instruments, Inc.1995-01-10
RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM (K941781)Dacomed Corp.1994-08-25
RT2 RIGIDITY AND TUMESCENCE TEST (K925931)Compass Medical Technologies, Inc.1992-12-21
BARD (R) ESKA ERECTIOMETER (K880903)C.R. Bard, Inc.1988-05-06
SURGITEK NPT MONITOR (K875333)Surgitek1988-04-13

Recalls involving this device

No recalls on record reference this clearance.