Electronic Insufflator, Model No. 2054.60

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K882185 ↗

FDA Product Code

HIF

Device Class

Class II

Regulation

21 CFR Part 884.1730

Advisory Committee

Obstetrics/Gynecology

FDA Decision

SESE Substantially Equivalent

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  Class II

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  Class II

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