MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50— 510(k) K980980
Substantially EquivalentKonigsberg Instruments, Inc.
FDA 510(k) clearance K980980 for MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50, Substantially Equivalent on 1998-06-15. Applicant: Konigsberg Instruments, Inc.. Device class: 2.
Clearance details
- Applicant
- Konigsberg Instruments, Inc.
- Product code
- Code FFX
- Device class
- Class 2
- Regulation
- 21 CFR 876.1725
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Pasadena, CA, US
Recent devices under product code FFX
view allMore clearances from Konigsberg Instruments, Inc.
view allAdverse events under product code FFX
product code FFX- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.