REMOLDABLE CRANIOMANDIBULAR APPLIANCE— 510(k) K833455

Substantially Equivalent

Jeffrey H. Attlin

FDA 510(k) clearance K833455 for REMOLDABLE CRANIOMANDIBULAR APPLIANCE, Substantially Equivalent on 1984-01-10. Applicant: Jeffrey H. Attlin.

Clearance details

Applicant: Jeffrey H. Attlin
Product code: Code KMY
Advisory panel: Dental
Date received: 1983-09-27
Decision date: 1984-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code KMY

product code KMY

Injury: 1,457
Total: 1,457

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.