FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCER— 510(k) K073664

Substantially Equivalent

Injectimed, Inc.

FDA 510(k) clearance K073664 for FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCER, Substantially Equivalent on 2008-08-08. Applicant: Injectimed, Inc..

Clearance details

Applicant: Injectimed, Inc.
Product code: Code MDM
Advisory panel: General, Plastic Surgery
Date received: 2007-12-26
Decision date: 2008-08-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Albuquerque, NM, US

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Adverse events under product code MDM

product code MDM

Injury: 247
Malfunction: 1,516
Total: 1,763

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.