Storz DP4101 Basic I/a Pack

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K953078 ↗

FDA Product Code

HQC

Device Class

Class II

Regulation

21 CFR Part 886.4670

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

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• Storz Premiere/Premiere Microvit Microsurg Systems

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