VIBRECTOR— 510(k) K851646

Substantially Equivalent

Multicept, Aps.

FDA 510(k) clearance K851646 for VIBRECTOR, Substantially Equivalent on 1985-08-21. Applicant: Multicept, Aps.. Device class: Unclassified.

Clearance details

Applicant: Multicept, Aps.
Product code: Code LIL
Device class: Unclassified
Advisory panel: Unknown
Date received: 1985-04-19
Decision date: 1985-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Copenhagen, DK

Download summary PDF View on FDA.gov ↗

Recent devices under product code LIL

K061676 — RIGIDOMETER, MODEL DIR-4U2006-12-27
K062042 — PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM)2006-09-06
K052929 — PREFTEST PROFESSIONAL SUITE2006-04-26
K033126 — MONARCH 21 PENILE PLETHYSMOGRAPH SYSTEM2003-10-29
K000194 — DIGITAL INFLECTION RIGIDOMETER (DIR)2000-04-10

More clearances from Multicept, Aps.

K955589 — FERTICARE PERSONAL THERAPEUTIC VIBRATOR1996-04-11

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