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ARGON ACUTE HEMODYLASIS KIT
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 Contact Information
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| Company Name | ARGON MEDICAL DEVICES INC. |
| Address | 1445 FLAT CREEK RD. |
| City, State, Zip | ATHENS, TX 75751 |
| Country | US |
| FDA Owner/Operator Phone | 903-675-9321 |
| FDA Medical Specialty Code | GU - Gastroenterology/Urology |
| FDA Product Code | FKO |
| FDA Classification Name | CATHETER, PERITONEAL DIALYSIS, SINGLE USE |
| FDA Device Classification Code | Standards |
| FDA Regulation Number | 876.5630 |
| FDA Common Generic Name | ACUTE HEMODIALYSIS KIT |
| FDA Proprietary Device Name | ARGON ACUTE HEMODYLASIS KIT |
| FDA Owner / Operator Number | 9059795 |
| FDA Owner / Operator Name | ARGON MEDICAL DEVICES, INC |
| FDA Establishment Registration Number | 1625425 |
| FDA Registered Establishment Name | ARGON MEDICAL DEVICES INC. |
| FDA Operation Code(s) |
MM - Manufacturer MR - Remanufacturer RR - Repackager/Relabeller |
| FDA Listing Date | 01-09-93 |
| FDA Listing Status Code | Active |
| Differentiation | N/A |
| Keywords | N/A |
| Description | N/A |
| Brochure | N/A |
| Product Website | N/A |
Competitors of ARGON MEDICAL DEVICES INC.
Our records indicate that the following medical device companies may manufacture a similar device.
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