PERCUTANEOUS INTRODUCER KIT— 510(k) K902135

Unknown

Device Labs, Inc.

FDA 510(k) clearance K902135 for PERCUTANEOUS INTRODUCER KIT, Unknown on 1990-08-01. Applicant: Device Labs, Inc..

Clearance details

Applicant: Device Labs, Inc.
Product code: Code FOZ
Advisory panel: General Hospital
Date received: 1990-05-10
Decision date: 1990-08-01
Decision: Unknown
Clearance type: Traditional
Location: Medway, MA, US

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Adverse events under product code FOZ

product code FOZ

Death: 38
Injury: 2,290
Malfunction: 25,858
Other: 11
Total: 28,197

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.