Identity
- Trade Name
- Luminscan(TM) Disposable Imaging Kit FDA UDI
- Generic Name
- Coronary optical coherence tomography system FDA UDI
- Device Name
- The diameter of the balloon is 20mm, the effective length is 30mm, the outer diameter of the Balloon catheter is 7Fr, and the length of the probe is 2500mm FDA UDI
- Model / Reference
- BOP-20-30-25-7 FDA UDI
- Description
- The diameter of the balloon is 20mm, the effective length is 30mm, the outer diameter of the Balloon catheter is 7Fr, and the length of the probe is 2500mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06932503570084 FDA UDI
- 510(k) Number
- K162466 FDA UDI
- FDA Product Code
- NQQ FDA UDI
- GMDN Term
- Coronary optical coherence tomography system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1560 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Balloon Diameter — 20 Millimeter FDA UDIBalloon Length — 30 Millimeter FDA UDILength — 250 Centimeter FDA UDI
Category: Coronary optical coherence tomography system
Luminscan(TM) Disposable Imaging Kit by Micro-Tech (Nanjing) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Coronary optical coherence tomography system.
- OPTIS™ — LIGHTLAB IMAGING, INC. · Class II
- OPTIS™ — ST. JUDE MEDICAL, INC. · Class II
- ILUMIEN™ — LIGHTLAB IMAGING, INC. · Class II
- ILUMIEN™ OPTIS™ to OPTIS™ — LIGHTLAB IMAGING, INC. · Class II
- OPTIS™ — LIGHTLAB IMAGING, INC. · Class II
- OPTIS™ — LIGHTLAB IMAGING, INC. · Class II
- OPTIS™ — ST. JUDE MEDICAL, INC. · Class II
- Gentuity — Gentuity, LLC · Class II
Cleared under the same submission
K162466 also covers:
- LuminScan(TM) Imaging System — Micro-Tech (Nanjing) Co., Ltd.
- Luminscan(TM) Disposable Imaging Kit — Micro-Tech (Nanjing) Co., Ltd.
- Luminscan(TM) Disposable Imaging Kit — Micro-Tech (Nanjing) Co., Ltd.
- Luminscan(TM) Disposable Imaging Kit — Micro-Tech (Nanjing) Co., Ltd.
- Luminscan(TM) Disposable Imaging Kit — Micro-Tech (Nanjing) Co., Ltd.
- Luminscan(TM) Disposable Imaging Kit — Micro-Tech (Nanjing) Co., Ltd.
- Luminscan(TM) Disposable Imaging Kit — Micro-Tech (Nanjing) Co., Ltd.
- Luminscan(TM) Disposable Imaging Kit — Micro-Tech (Nanjing) Co., Ltd.
- Luminscan(TM) Disposable Imaging Kit — Micro-Tech (Nanjing) Co., Ltd.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Micro-Tech (Nanjing) Co., Ltd.
Sources (1)
- FDA UDI 476994c3-50ca-4434-9134-2753f4f41a73 36 fields · synced Jun 8, 2026