Nidoil
FDA 510(k) K012123 · Nidacon International AB
510(k) numberK012123
Submission
- Device name
- Nidoil
- Applicant
- Nidacon International AB
Deer Field, IL, US - Received
- July 6, 2001
- Decision date
- August 3, 2001
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MQL – Media, Reproductive
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.6180
- Specialty
- Obstetrics/Gynecology
Other 510(k)s with product code MQL
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K254261 | Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK)MQL · Traditional | Cell Store (Beijing) Biotechnology Co., Ltd. | 08/28/2026SE |
| K260248 | Ultra-Fast WarmMQL · Traditional | Kitazato Corporation | 04/28/2026SE |
| K252672 | CaseBio Culture w/HSA (CMH5); CaseBio Handling w/HSA (WHH5)MQL · Traditional | Casebioscience, Inc. | 02/20/2026SE |
| K250445 | Fast Warm - NXMQL · Traditional | Fujifilm Irvine Scientific | 09/12/2025SE |
| K251637 | Dewin Reproductive Media (Dewin Gamete Buffer [with HSA and without HSA]; Dewin Follicle…MQL · Traditional | Donnevie Medical Technology (Shanghai) Co. , Ltd. | 08/27/2025SE |
| K251305 | Ultra-Fast Vitri; Ultra-Fast WarmMQL · Traditional | Kitazato Corporation | 08/26/2025SE |
| K242640 | FertiCult Flushing medium; FertiCult Flushing medium with phenol red and gentamicinMQL · Traditional | Fertipro NV | 05/30/2025SE |
| K242561 | Dewin Reproductive Media (Dewin Vitrification Kit, Dewin Thawing Kit)MQL · Traditional | Donnevie Medical Technology (Shanghai) Co. , Ltd. | 04/10/2025SE |
| K242089 | Vitrification Freeze Kit (RFD-0101) Vitrification Thaw Kit (RFD-0201, RFD-0202)MQL · Traditional | Jiangsu Ruifuda Medical Device Co., Ltd. | 04/10/2025SE |
| K242107 | CaseMONO Culture (CMON); CaseMONO w/HEPES (WHMO); CaseBioscience® HTF (HTFC)…MQL · Traditional | Casebioscience, Inc. | 03/21/2025SE |
More from Casebioscience, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K131145 | ProinsertMQK · Traditional | 02/20/2014SE |
| K092107 | Vitriblast, Thermoblast, Model VB-010, TB-010MQL · Traditional | 06/15/2010SE |
| K023206 | Sperm CryoprotecMQL · Traditional | 11/08/2002SE |
| K022443 | SpermassistMQL · Traditional | 08/28/2002SE |
| K011607 | SpermcatchMQL · Traditional | 08/10/2001SE |
| K011606 | Puresperm BufferMQL · Traditional | 07/12/2001SE |
| K011346 | ReadyswimMQL · Traditional | 06/28/2001SE |
| K002630 | Puresperm WashMQL · Traditional | 11/21/2000SE |
| K002623 | Puresperm 40 and Puresperm 80MQL · Traditional | 11/20/2000SE |
| K984172 | Modification of PurespermMQL · Traditional | 01/14/1999SE |
Questions and answers
When was Nidoil cleared by the FDA?
Nidoil (K012123) received a 510(k) decision of Substantially Equivalent on August 3, 2001, 28 days after the submission was received.
What is the product code of K012123?
The FDA product code is MQL – Media, Reproductive, a Class II (moderate risk) device regulated under 21 CFR 884.6180.