Superlogger
FDA 510(k) K912772 · Sandhill Scientific, Inc.
510(k) numberK912772
Submission
- Device name
- Superlogger
- Applicant
- Sandhill Scientific, Inc.
Littleton, CO, US - Received
- June 24, 1991
- Decision date
- February 7, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FFT – Electrode, Ph, Stomach
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 876.1400
- Specialty
- Gastroenterology, Urology
Other 510(k)s with product code FFT
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K102543 | Bravo PH Monitoring System and AccessoriesFFT · Traditional | Given Imaging , Ltd. | 12/01/2010SE |
| K013951 | Sandhill Scientific Pediatec PH ProbeFFT · Traditional | Sandhill Scientific, Inc. | 02/28/2002SE |
| K002028 | Bravo PH Monitoring SystemFFT · Traditional | Endonetics, Inc. | 09/29/2000SE |
| K961346 | PH Analysis ModuleFFT · Traditional | Synectics-Dantec | 01/29/1997SE |
| K950087 | Lot 440FFT · Traditional | Medical Instruments Corporation Mic AG | 02/06/1996SE |
| K955018 | Trip NGS & Sigmoid Catheter Phi Slide CalculatorFFT · Traditional | Instrumentarium Corp. | 01/30/1996SE |
| K945069 | Flexilog 2000FFT · Traditional | Oakfield Instruments, Ltd. | 06/13/1995SE |
| K920849 | Trip Cic CatheterFFT · Traditional | Tonometrics, Inc. | 03/17/1995SE |
| K934434 | Cyberrx Model 7200FFT · Traditional | Cybermed Control Systems, Inc. | 01/24/1995SE |
| K925405 | Zinetics Composite Sensor Probe W/Internal Ref.FFT · Traditional | Synectics-Dantec | 09/30/1994SE |
More from Synectics-Dantec
| 510(k) | Device | Decision |
|---|---|---|
| K111013 | AcemFFZ · Traditional | 12/19/2011SE |
| K012232 | Insight, Model S980000FFX · Traditional | 06/07/2002SE |
| K013951 | Sandhill Scientific Pediatec PH ProbeFFT · Traditional | 02/28/2002SE |
| K002427 | Sandhill Unitip Catheter Pressure Sensor, Model K 5251-L3-0026FFX · Abbreviated | 06/22/2001SE |
| K990441 | Insight Sphincter of Oddi Manometry Module, Model S981300FFX · Traditional | 05/12/1999SE |
| K984444 | Insight Gastrointestinal Motility System, Model S980000FFX · Special | 01/11/1999SE |
| K961056 | Bioview Model S960000KLA · Traditional | 06/06/1996SE |
| K942247 | Small Bowel Analysis SoftwareFFX · Traditional | 04/09/1996SE |
| K941801 | AnalgraphKLA · Traditional | 09/08/1995SE |
| K931963 | Sandhill Disposable Internal Reference PH ProbeFFT · Traditional | 09/28/1994SE |
Questions and answers
When was Superlogger cleared by the FDA?
Superlogger (K912772) received a 510(k) decision of Substantially Equivalent on February 7, 1992, 228 days after the submission was received.
What is the product code of K912772?
The FDA product code is FFT – Electrode, Ph, Stomach, a Class I (low risk) device regulated under 21 CFR 876.1400.