MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50— 510(k) K980980

Substantially Equivalent

Konigsberg 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..

Clearance details

Applicant: Konigsberg Instruments, Inc.
Product code: Code FFX
Advisory panel: Gastroenterology, Urology
Date received: 1998-03-17
Decision date: 1998-06-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pasadena, CA, US

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Adverse events under product code FFX

product code FFX

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.