Data / Medical devices / Taiwan / Cheen Houng Ent. Co. Ltd.
Cheen Houng Ent. Co. Ltd.: FDA-registered device maker in SHULIN Taipei, Taiwan, 2 510(k) clearances
Cheen Houng Ent. Co. Ltd. is registered with the FDA (registration 9612374) in SHULIN Taipei, Taiwan. It lists 5 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 14, 2001. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9612374
- FEI number
- 3002806674
- Address
- 23, Alley 11, Lane 65 San Dreen ST., SHULIN Taipei, Taiwan, 23805
- Owner or operator
- CHEEN HOUNG ENT. CO. LTD. (8043061)
- Roles
- Contract manufacturer, Exporter to the US, Specification developer
- First device listed
- July 27, 2005
- Registered through
- 2026
- Brand names listed
- 22/10mm Tube, CPR bag accessory(LiteSaver), Face Cradle, PEEP VALVE, Pocket Mask
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Attachment, Breathing, Positive End Expiratory Pressure | BYE | 2 | Specification developer | accessdata.fda.gov |
| Support, Patient Position | CCX | 1 | Contract manufacturer | accessdata.fda.gov |
| Tubing, Pressure And Accessories | BYX | 1 | Exporter to the US | accessdata.fda.gov |
| Valve, Non-Rebreathing | CBP | 2 | Specification developer | accessdata.fda.gov |
| Ventilator, Emergency, Manual (Resuscitator) | BTM | 2 | Contract manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 14, 2001 | K010191 | Y2000 POCKET RESCUE | CBP | Substantially Equivalent | Cheen Houng Ent. Co. , Ltd. | accessdata.fda.gov |
| July 14, 1998 | K981415 | 0-20 CM H20 PEEP VALVE | BYE | Substantially Equivalent | Cheen Houng Ent. Co. , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Tubing, Pressure And Accessories
- All makers of Support, Patient Position
- All makers of Valve, Non-Rebreathing
- All makers of Ventilator, Emergency, Manual (Resuscitator)
- All makers of Attachment, Breathing, Positive End Expiratory Pressure
Updated March 14, 2001. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.