RI MSC (MIGRATION SEDIMENTATION CHAMBER)— 510(k) K112413

Name: FDA 510(k) clearance K112413
Creator: U.S. Food and Drug Administration
Published: 2012-07-13

Substantially Equivalent

Research Instruments , Ltd.

FDA 510(k) clearance K112413 for RI MSC (MIGRATION SEDIMENTATION CHAMBER), Substantially Equivalent on 2012-07-13. Applicant: Research Instruments , Ltd.. Device class: 2.

Clearance details

Applicant: Research Instruments , Ltd.
Product code: Product code MQK
Device class: Class 2
Regulation: 21 CFR 884.6160
Advisory panel: Obstetrics/Gynecology
Date received: 2011-08-22
Decision date: 2012-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Falmouth, Cornwall, GB

Download summary PDF View on FDA.gov ↗

Recent devices under product code MQK

view all

K262066 — Pleiades Device2026-10-30
K262276 — Cyperus2026-10-26
K262090 — Fertilis microICSI Device2026-10-09
K241626 — SperSort Sperm Sorting Chip (IPG02)2025-02-20
K241454 — Minvitro® Vitrification Straw (MVT-VSN series, including MVT-VSNR, MVT-VSNY, MVT-VSNB, MVT-VSNG, MVT-VSNP)2025-02-03

More clearances from Research Instruments , Ltd.

view all

K141434 — SATURN 5 LASER2015-02-18
K133257 — BIOPSY PIPETTES2014-05-16
K083208 — SATURN ACTIVE LASER SYSTEM2009-08-25
K060764 — SATURN 3 LASER SYSTEM2007-03-12
K003142 — MICROMANIPULATOR2000-11-22

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