EROS-CLITORAL THERAPY DEVICE (CTD)— 510(k) DEN000006

Unknown

Urometrics, Inc.

FDA 510(k) clearance DEN000006 for EROS-CLITORAL THERAPY DEVICE (CTD), Unknown on 2000-04-28. Applicant: Urometrics, Inc.. Device class: 2.

Clearance details

Applicant: Urometrics, Inc.
Product code: Code NBV
Device class: Class 2
Regulation: 21 CFR 884.5970
Advisory panel: Obstetrics/Gynecology
Date received: 2000-04-27
Decision date: 2000-04-28
Decision: Unknown
Clearance type: Post-NSE
Location: St. Paul, MN, US

View on FDA.gov ↗

Recent devices under product code NBV

K043480 — ENHANCE CLITORAL STIMULATION AID2005-06-08
K001576 — EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY2000-12-28

More clearances from Urometrics, Inc.

K980627 — NEVA SYSTEM1998-04-07
K971790 — KNOLL/MIDUS (MALE IMPOTENCE DIAGNOSTIC ULTRASONIC SYSTEM)1997-12-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.