DR GREENBURGS HYBRID VACUUM— 510(k) K120372

Substantially Equivalent

Always More Marketing, Inc.

FDA 510(k) clearance K120372 for DR GREENBURGS HYBRID VACUUM, Substantially Equivalent on 2012-06-27. Applicant: Always More Marketing, Inc..

Clearance details

Applicant: Always More Marketing, Inc.
Product code: Code LRK
Advisory panel: Dental
Date received: 2012-02-06
Decision date: 2012-06-27
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Las Vegas, NV, US

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Adverse events under product code LRK

product code LRK

Injury: 246
Malfunction: 1,044
Total: 1,290

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.