Rapidec Ur
FDA 510(k) K894805 · Dms Products, Inc.
510(k) numberK894805
Submission
- Device name
- Rapidec Ur
- Applicant
- Dms Products, Inc.
Flemington, NJ, US - Received
- July 28, 1989
- Decision date
- September 26, 1989
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- JXA – Kit, Screening, Urine
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.2660
- Specialty
- Microbiology
Other 510(k)s with product code JXA
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K011043 | Osmetech Microbial Analyser-Urinary Tract Infection Detector (Oma-Uti)JXA · Traditional | Osmetech | 11/30/2001SE |
| K981084 | UriscreenJXA · Traditional | Diatech Diagnostics,Inc. | 10/07/1998SE |
| K972676 | Urine Screening DeviceJXA · Traditional | Combact Diagnostic Systems , Ltd. | 02/23/1998SE |
| K952246 | Tri-Techin. Custom Blood And/Or Urine Transport KitJXA · Traditional | Tri-Tech, Inc. | 06/20/1995SE |
| K950257 | Multiple (Izon DBS & Urine Collection Kit)JXA · Traditional | Izon Business Products, Inc. | 04/14/1995SE |
| K950246 | Multiple (Izon Urine Collection Kit)JXA · Traditional | Izon Business Products, Inc. | 03/21/1995SESK |
| K950221 | Multiple (Izon Blood & Urine Collection Kit)JXA · Traditional | Izon Business Products, Inc. | 03/21/1995SEKD |
| K934759 | Culturia Macconkey-MugJXA · Traditional | Clinical Convenience Products, Inc. | 09/09/1994SE |
| K924218 | Bac-T-ScreenJXA · Traditional | Biomerieux Vitek, Inc. | 02/03/1993SE |
| K921045 | Diaslide Urine Culturing DeviceJXA · Traditional | Savyon Diagnostics , Ltd. | 09/28/1992SE |
More from Savyon Diagnostics , Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K891004 | Rapidec StaphLQL · Traditional | 11/09/1989SE |
| K890626 | Rapidec ColiJSS · Traditional | 06/02/1989SE |
| K890625 | James ReagentJTO · Traditional | 02/17/1989SE |
| K854733 | Api 20 Ec (Enterobacteriaceae)(Identification Kit)JSS · Traditional | 03/06/1986SE |
| K854732 | Api 50 CHB (Culture Media)JST · Traditional | 03/04/1986SE |
Questions and answers
When was Rapidec Ur cleared by the FDA?
Rapidec Ur (K894805) received a 510(k) decision of Substantially Equivalent on September 26, 1989, 60 days after the submission was received.
What is the product code of K894805?
The FDA product code is JXA – Kit, Screening, Urine, a Class I (low risk) device regulated under 21 CFR 866.2660.