Apk I-A1501-SW245PU
Active
510(k)
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06946725517154 | Date12 Mar 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK082846 | Date3 Apr 2009 | StatusActive |
Recalls
No FDA recalls found in the data synced 9 Nov 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Apk
- Generic name
- Pulse oximeter probe, reusable
- Model / Ref / Catalog
- I-A1501-SW245PU, A1501-SW245PU
- Primary DI / UDI-DI
- 06946725517154
- 510(k) Number
- FDA product code
- DQA
- GMDN term
- Pulse oximeter probe, reusable
- Device class
- Class II
- Regulation number
- 870.2700
- GUDID distribution status
- In Commercial Distribution
Other devices from APK Technology Co., Ltd.
Properties
Other properties (13)
- Supplied sterile: No
- Sterilise before use: No
- Single use: No
- Implantable: No
- Contains latex: No
- Prescription use: No
- Over-the-counter: No
- Convenience kit: No
- Combination product: No
- HCT/P: No
- Premarket exempt: No
- Lot / batch number: No
- Expiration date: No