REXTAR X— 510(k) K132041

Substantially Equivalent

Meta Biomed, Inc.

FDA 510(k) clearance K132041 for REXTAR X, Substantially Equivalent on 2013-07-31. Applicant: Meta Biomed, Inc.. Device class: 2.

Clearance details

Applicant: Meta Biomed, Inc.
Product code: Code EHD
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2013-07-02
Decision date: 2013-07-31
Decision: Substantially Equivalent
Clearance type: Special
Location: Mt. Airy, MD, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EHD

K260367 — Portable Dental X-ray System Model PDX nova2026-05-27
K253864 — NOMAD Pro 32026-03-20
K252110 — Dental X-RAY Unit (AJX200)2026-03-12
K254018 — Portable Dental X-ray Device (GT-1)2026-02-19
K252909 — Diagnostic X-Ray Equipment Model POCT222026-02-03

More clearances from Meta Biomed, Inc.

Data sourced from openFDA. This site is unofficial and independent of the FDA.