← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS III

GZE — Implanted Diaphragmatic/Phrenic Nerve Stimulator

Call for pmas to be filed by 7/7/86 per 51 fr 12101 on 4/8/86

DEVICE CLASS
Class III
REGULATION
21 CFR 882.5830
MEDICAL SPECIALTY
Neurology
REVIEW PANEL
AN
✓ Implant— Life-sustaining— GMP-exempt— Third-party review eligible
0
510(K)/PMA CLEARANCES
0
RECALL ENTRIES

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 →