Espi Micro Grasper, Double-Action, Insulated, #8250-N

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K903600 ↗

FDA Product Code

HET

Device Class

Class II

Regulation

21 CFR Part 884.1720

Advisory Committee

Obstetrics/Gynecology

FDA Decision

SESE Substantially Equivalent

• Espi Reducer Sleeve, #8415

  Class II

  FDA 510(k) K903596 Active Cleared 12 Sep 1990

• Espi Micro Scissors, #8150

  Class II

  FDA 510(k) K903597 Active Cleared 12 Sep 1990

• Espi Hook/Universal Scissors, # 8101

  Class II

  FDA 510(k) K903591 Active Cleared 12 Sep 1990

• Espi Non-Insulated Double-Action Grasper, #8203

  Class II

  FDA 510(k) K903602 Active Cleared 12 Sep 1990

• Espi Double-Action Insulated Grasper, #8203-N

  Class II

  FDA 510(k) K903599 Active Cleared 17 Oct 1990

• Espi Claw Forcep, #8301, 5mm, 30 Cm Length

  Class II

  FDA 510(k) K903592 Active Cleared 12 Sep 1990

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