HUMAN TUBAL FLUID— 510(k) K953719

Substantially Equivalent

Life Technologies, Inc.

FDA 510(k) clearance K953719 for HUMAN TUBAL FLUID, Substantially Equivalent on 1995-11-06. Applicant: Life Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Life Technologies, Inc.
Product code: Code MFD
Device class: Class 2
Regulation: 21 CFR 884.5250
Advisory panel: Obstetrics/Gynecology
Date received: 1995-08-09
Decision date: 1995-11-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Island, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MFD

K021438 — INSEMINATION CATHETER, MODEL 3203012002-07-16
K012935 — THECURVE, ITEM 5072001-10-11
K984306 — `THE INSEMINATOR' (PROPOSED)1999-03-01
K982630 — MEDWORKS VISUALIZATION INSEMINATION CATHETER1999-01-14
K982628 — MEDWORKS INSEMINATION CATHETER1998-08-21

More clearances from Life Technologies, Inc.

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