Pocketcpr
Pocketcpr, Includes CR123 Lithium Battery With 5 Year Shelf Life
2manufacturers in China registered for this device type
3catalogue numbers in this listing
1510(k) clearance
Who Else Makes It
All of them in Guangdong. 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Amphenol Medical Technologies (Dongguan) Co., Ltd. | Dongguan | Guangdong | Contract manufacturer | 77 |
| Amphenol Alden Products Company | Shenzhen | Guangdong | Contract manufacturer | 24 |
Record
| Listed by | Zoll Medical Corporation, United States |
|---|---|
| FDA product code | LIX |
| Device type | Aid, Cardiopulmonary Resuscitation |
| Device class | Class 2 |
| Regulation | 21 CFR 870.5210 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer |
| Record published | 2014-09-24 |
| Record revised | 2026-02-16 (version 6) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Label carries | lot or batch number, serial number |
| Storage | Storage environment humidity 15 to 95 % RH; Storage environment temperature -30 to 65 °C |
| Distribution end date | 2026-01-01 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 8900-1500-01 | 9.4″ X 6.1″ X 2.8″ | Withdrawn |
| 8900-001500-10 | 9.4″ X 6.1″ X 2.8″ | Withdrawn |
| 8900-001500-05 | 9.4″ X 6.1″ X 2.8″ | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Moore Medical | Moore Medical Corp. | 2 |
| TrueCPR™ Coaching Device | Physio-Control, Inc. | 2 |
| Intellisense Adult Defibrillation Pads,CPR Device, Powerheart® G5 | Zoll Medical Corporation | 1 |
| CPRmeter 2 (Multi-bundle) | Laerdal Medical Corp. | 1 |
| CPRmeter | Laerdal Medical Corp. | 1 |
| Onestep Pediaric CPR Multi-Function Electrode, SIN | Zoll Medical Corporation | 1 |
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K112660 | 2012-05-10 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.