GOULD XCALIBER— 510(k) K862344

Substantially Equivalent

Bio-Tek Instruments, Inc.

FDA 510(k) clearance K862344 for GOULD XCALIBER, Substantially Equivalent on 1986-08-06. Applicant: Bio-Tek Instruments, Inc..

Clearance details

Applicant: Bio-Tek Instruments, Inc.
Product code: Code DRS
Advisory panel: Cardiovascular
Date received: 1986-06-20
Decision date: 1986-08-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Winooski, VT, US

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Adverse events under product code DRS

product code DRS

Death: 8
Malfunction: 776
Total: 784

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.