Abc Laparoscopic Handprobe

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K910889 ↗

FDA Product Code

GEI

Device Class

Class II

Regulation

21 CFR Part 878.4400

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Birtcher Laparoscope and Accessories

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  FDA 510(k) K932987 Active Cleared 25 Apr 1994

• Birtcher Swivel Grip Laparoscopic Probes & Access.

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  FDA 510(k) K932779 Active Cleared 21 Mar 1995

• Birtcher Bronchus & Lung Clamp (Gs-1620 & Gs-1600)

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• Birtcher Magnetic Retriever (Gs-3100)

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• Laparoscopic 5MM ABC Probe, Modification

  Class II

  FDA 510(k) K925903 Active Cleared 30 Dec 1992

See all devices from Birtcher Medical Systems, Inc. →