MITYVAC DIRECTIONAL VACUUM EXTRACTOR, DISPOSABLE— 510(k) K960549

Substantially Equivalent

Neward Enterprises, Inc.

FDA 510(k) clearance K960549 for MITYVAC DIRECTIONAL VACUUM EXTRACTOR, DISPOSABLE, Substantially Equivalent on 1996-08-29. Applicant: Neward Enterprises, Inc..

Clearance details

Applicant: Neward Enterprises, Inc.
Product code: Code HDB
Advisory panel: Obstetrics/Gynecology
Date received: 1996-02-08
Decision date: 1996-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cucamonga, CA, US

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Adverse events under product code HDB

product code HDB

Death: 7
Total: 7

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.