MICROMANIPULATOR— 510(k) K003142

Substantially Equivalent

Research Instruments , Ltd.

FDA 510(k) clearance K003142 for MICROMANIPULATOR, Substantially Equivalent on 2000-11-22. Applicant: Research Instruments , Ltd.. Device class: 2.

Clearance details

Applicant: Research Instruments , Ltd.
Product code: Code MQJ
Device class: Class 2
Regulation: 21 CFR 884.6150
Advisory panel: Obstetrics/Gynecology
Date received: 2000-10-10
Decision date: 2000-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Penryn, Corwall, GB

Download summary PDF View on FDA.gov ↗

Recent devices under product code MQJ

K142207 — TransferMan 4m Micromanipulator2015-01-23
K120877 — MICROMANIPULATOR SET2012-06-20
K113712 — IM-11 PNEUMATIC MICROINJECTOR2012-03-15
K011420 — MM-87 MOTOR-DRIVE MANIPULATOR2001-06-12
K010298 — MN-4 COARSE MANIPULATOR2001-03-16

More clearances from Research Instruments , Ltd.

K141434 — SATURN 5 LASER2015-02-18
K133257 — BIOPSY PIPETTES2014-05-16
K112413 — RI MSC (MIGRATION SEDIMENTATION CHAMBER)2012-07-13
K083208 — SATURN ACTIVE LASER SYSTEM2009-08-25
K060764 — SATURN 3 LASER SYSTEM2007-03-12

Recalls naming K003142

K-number listed on FDA's recall record

Z-1584-2016 — Integra 3; Model Numbers: 6-54-100, 6-54-110, 6-54-150, 6-54-160 Product Usage: The Rl TDU500 Micromanipulator for Assisted Reproduction is used to accurately position microtools under a microscope for the techniques of Assisted Reproduction. The Rl Integra is a configuration comprising two TDU500 micromanipulators, two air syringes and temperature control system within a single housing.Class II·Terminated·RESEARCH INSTRUMENTS LTD - SITE B·20160311

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K003142.

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