HARVEST TECHNOLOGIES DUAL LIQUID APPLICATOR, MODEL SK/S: HARVEST DUAL LIQUID APPLICATOR LK/2— 510(k) K000456

Substantially Equivalent

Harvest Technologies, LLC

FDA 510(k) clearance K000456 for HARVEST TECHNOLOGIES DUAL LIQUID APPLICATOR, MODEL SK/S: HARVEST DUAL LIQUID APPLICATOR LK/2, Substantially Equivalent on 2000-06-01. Applicant: Harvest Technologies, LLC.

Clearance details

Applicant: Harvest Technologies, LLC
Product code: Code FMF
Advisory panel: General Hospital
Date received: 2000-02-11
Decision date: 2000-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwell, MA, US

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Adverse events under product code FMF

product code FMF

Death: 15
Injury: 2,263
Malfunction: 29,722
Other: 17
Total: 32,017

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.