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Sign in to claim this brandChongqing Psk Sci-Tech Development Co., Ltd.
US
Last updated May 23, 2026
What Chongqing Psk Sci-Tech Development Co., Ltd. makes
Chongqing Psk Sci-Tech Development Co., Ltd. makes an external counterpulsation device with SpO2 monitoring.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What type of device does Chongqing Psk Sci-Tech Development Co., Ltd. make?
Chongqing Psk Sci-Tech Development Co., Ltd. makes an external counterpulsation device with SpO2 monitoring, as stated in the device data summary. This is the only example device provided, and no other products are mentioned or implied.
Where is Chongqing Psk Sci-Tech Development Co., Ltd. based?
The company is based in the United States, as explicitly stated in the SUMMARY section of the device data. The COUNTRY field also confirms this as US, and no other location is referenced.
In which regulatory registry is Chongqing Psk Sci-Tech Development Co., Ltd.'s device listed?
The device is listed in the FDA 510(k) registry, as indicated in the LISTED IN field and reiterated in the SUMMARY. This is the only registry mentioned for the company's device.
How is Chongqing Psk Sci-Tech Development Co., Ltd.'s device classified?
The device is classified as Class II, as specified in the DEVICE CLASSES field and confirmed in the SUMMARY. Classification refers to the device's risk level under regulatory frameworks, not company approval.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
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Catalogue (5)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| PSK, Air-bag Type Sequential External Counter-pulsation Device | PECP/TM | FDA UDI | Class II | Active |
| PSK, Air-bag Type Sequential External Counter-pulsation Device | PECP/TI | FDA UDI | Class II | Active |
| Ecp Psk | P-ECP/TI | FDA UDI | Class II | Unknown |
| Ecp Psk | P-ECP/TM | FDA UDI | Class II | Unknown |
| External Counterpulsation Device With Sp02 Mornitoring | K130439 | FDA 510(k) | Class II | Active |
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