MERISTEEL— 510(k) K172146

Name: FDA 510(k) clearance K172146
Creator: U.S. Food and Drug Administration
Published: 2018-02-01

Substantially Equivalent

M/s. Meril Endo Surgery Private Limited.

FDA 510(k) clearance K172146 for MERISTEEL, Substantially Equivalent on 2018-02-01. Applicant: M/s. Meril Endo Surgery Private Limited.. Device class: 2.

Clearance details

Applicant: M/s. Meril Endo Surgery Private Limited.
Product code: Code GAQ
Device class: Class 2
Regulation: 21 CFR 878.4495
Advisory panel: General, Plastic Surgery
Date received: 2017-07-17
Decision date: 2018-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chala, Vapi, IN

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GAQ

product code GAQ

Death: 3
Malfunction: 522
Total: 525

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.