LARVAL DEBRIDEMENT THERAPY PRODUCTS - LARVAE 100/200/300 AND BIOBAG 50/100/200/300/400— 510(k) K142020

Name: FDA 510(k) clearance K142020
Creator: U.S. Food and Drug Administration
Published: 2014-11-05

Substantially Equivalent

Biomonde

FDA 510(k) clearance K142020 for LARVAL DEBRIDEMENT THERAPY PRODUCTS - LARVAE 100/200/300 AND BIOBAG 50/100/200/300/400, Substantially Equivalent on 2014-11-05. Applicant: Biomonde. Device class: Unclassified.

Clearance details

Applicant: Biomonde
Product code: Code NQK
Device class: Unclassified
Advisory panel: Unknown
Date received: 2014-07-25
Decision date: 2014-11-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marlborough, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code NQK

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K131221 — LARVAL DEBRIDEMENT THERAPY PRODUCTS - BIOBAG 50/100/200/300/4002013-08-28
K123449 — BIOMONDE LARVAE2013-03-05
K102827 — MEDICAL MAGGOTS, LESOC2011-11-02
K072438 — MEDICAL MAGGOTS, CREATURE COMFORTS2007-10-05
K033391 — MEDICAL MAGGOTS2004-01-12

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