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FDA PRODUCT CODE · CLASS II

OHP — Expiratory Resistance Valve, Intranasal, For Obstructive Sleep Apnea

Intranasal device that creates expiratory resistance for the treatment of obstructive sleep apnea.

DEVICE CLASS
Class II
REGULATION
21 CFR 872.5570
MEDICAL SPECIALTY
Dental
REVIEW PANEL
DE
— 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.

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