Product code LIL— Unknown
DACOMED SNAP-GAUGE
- Classification name
- Monitor, Penile Tumescence
- Device class
- Unclassified
- Advisory panel
- Unknown
- Total cleared
- 26
- First cleared
- Most recent
Market context for product code LIL
FDA has cleared devices under product code LIL between 1981 and 2006, filed by 19 applicant companies. No FDA device recalls reference this product code.
Clearances per year
last 15 years- 2006
- 2003
- 2000
- 1999
- 1998
- 1995
- 1994
- 1992
- 1988
- 1987
- 1985
- 1984
- 1983
- 1982
- 1981
Top applicants under product code LIL
Recent clearances under product code LIL
- K061676 — RIGIDOMETER, MODEL DIR-4U
- K062042 — PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM)
- K052929 — PREFTEST PROFESSIONAL SUITE
- K033126 — MONARCH 21 PENILE PLETHYSMOGRAPH SYSTEM
- K000194 — DIGITAL INFLECTION RIGIDOMETER (DIR)
- K991479 — VISER PENILE TUMESCENCE MONITOR
- K980627 — NEVA SYSTEM
- K936115 — CAT-600 PENILE PLETHYSMOGRAPH
- K940128 — CAT-400UL PENILE PLETHYSMOGRAPH
- K941781 — RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM
- K925931 — RT2 RIGIDITY AND TUMESCENCE TEST
- K880903 — BARD (R) ESKA ERECTIOMETER
- K875333 — SURGITEK NPT MONITOR
- K870983 — NOCTURNAL PENILE TUMESCENCE MONITOR
- K851646 — VIBRECTOR
- K841879 — LFT - 212
- K841202 — DACOMED RIGISCAN SYSTEM
- K833454 — BIOREM 3000 & 4000
- K832121 — DACOMED SNAP-GAUGE
- K831251 — TUMISENSOR 1524
- K831252 — TUMISTORE RECORDER 1311
- K830221 — BEDSIDE N.P.T. 9900 - PRINTER 9800
- K830158 — OREXAS POTENTEST
- K822099 — BIOREM 2000
- K820615 — DACOMED SNAP-GAUGE
- K810944 — PENILE ERECTION MONITOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.