LKB 2160 MIDISPIN CENTRIFUGE— 510(k) K831947

Substantially Equivalent

Lkb Instruments, Inc.

FDA 510(k) clearance K831947 for LKB 2160 MIDISPIN CENTRIFUGE, Substantially Equivalent on 1983-07-29. Applicant: Lkb Instruments, Inc..

Clearance details

Applicant: Lkb Instruments, Inc.
Product code: Code JQC
Advisory panel: Clinical Chemistry
Date received: 1983-06-16
Decision date: 1983-07-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code JQC

product code JQC

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.