VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS— 510(k) K042074
Substantially EquivalentVanguard Medical Concepts, Inc.
FDA 510(k) clearance K042074 for VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS, Substantially Equivalent on 2005-03-09. Applicant: Vanguard Medical Concepts, Inc.. Device class: 2.
Clearance details
- Applicant
- Vanguard Medical Concepts, Inc.
- Product code
- Code NLH
- Device class
- Class 2
- Regulation
- 21 CFR 870.1220
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lakeland, FL, US
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More clearances from Vanguard Medical Concepts, Inc.
view all- K053051 — VANGUARD REPROCESSED EXTERNAL FIXATION DEVICES
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Recalls naming K042074
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K042074.
Data sourced from openFDA. This site is unofficial and independent of the FDA.