← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS II

NYV — Gastrointestinal Motility System, Capsule

Used to evaluate GI motility disorders and indicated for use in evaluating patients with suspected motility disorders.

DEVICE CLASS
Class II
REGULATION
21 CFR 876.1725
MEDICAL SPECIALTY
Gastroenterology, Urology
REVIEW PANEL
GU
— Implant— Life-sustaining— GMP-exempt— Third-party review eligible
3
510(K)/PMA CLEARANCES
510k: 3
0
RECALL ENTRIES

Recent clearances

K253569Atmo Biosciences, Ltd. · 510k2026-05-22
K250940Atmo Biosciences, Ltd. · 510k2025-06-26
K250493Anx Robotica Corporation · 510k2025-05-21

Related on SPEQ

Medical devices industry →Medical device quality (ISO 13485) →FDA device clearances →FDA enforcement & recalls →

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

Weekly Briefing

Get the Weekly GxP Briefing

Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.

Read a past issue →