← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS II

GWM — Device, Monitoring, Intracranial Pressure

DEVICE CLASS
Class II
REGULATION
21 CFR 882.1620
MEDICAL SPECIALTY
Neurology
REVIEW PANEL
NE
— Implant— Life-sustaining— GMP-exempt✓ Third-party review eligible
2
510(K)/PMA CLEARANCES
510k: 2
0
RECALL ENTRIES

Recent clearances

K252241Sophysa · 510k2026-04-10
K250285Raumedic AG · 510k2025-08-29

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.

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