PGD-PRE-IMPLANTATION GENETIC DIAGNOSTIC PIPETTES (BIOPSY PIPETTES)— 510(k) K014160
Substantially EquivalentCook Urological, Inc.
FDA 510(k) clearance K014160 for PGD-PRE-IMPLANTATION GENETIC DIAGNOSTIC PIPETTES (BIOPSY PIPETTES), Substantially Equivalent on 2002-02-08. Applicant: Cook Urological, Inc.. Device class: 2.
Clearance details
- Applicant
- Cook Urological, Inc.
- Product code
- Code MQG
- Device class
- Class 2
- Regulation
- 21 CFR 884.6120
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Spencer, IN, US
Recent devices under product code MQG
view all- K261083 — Wallace® Aspiration Pump (WAPV1); Wallace® Pump Filter Connector (WFC); Wallace® Vacuum Connection Kit (WVCK)
- K260194 — Vacuum Pump (Model: AD-VPUM-500)
- K242684 — Harioculture TL-16 Time-lapse Incubator
- K232493 — Embryo Real-time Incubator (TLS301), Embryo Real-time Culture Dish (MC 2004)
- K180188 — Geri Embryo Incubator with Geri Connect and Geri Assess Software, and Geri Dish
More clearances from Cook Urological, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.