PATIENT EXAMINATION GLOVES— 510(k) K893606

Substantially Equivalent

Aukland Mfg., Inc.

FDA 510(k) clearance K893606 for PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1990-03-09. Applicant: Aukland Mfg., Inc..

Clearance details

Applicant: Aukland Mfg., Inc.
Product code: Code LZA
Advisory panel: General Hospital
Date received: 1989-05-10
Decision date: 1990-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cary, NC, US

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Adverse events under product code LZA

product code LZA

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.