Hatcher Stone-Embolis Extractor

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K931115 ↗

FDA Product Code

LQR

Device Class

Class II

Regulation

21 CFR Part 876.5010

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

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  FDA 510(k) K891021 Active Cleared 18 Sep 1989

• Ideas' Port

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  Class II

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• Grice Laparoscopic Suturing Needle

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  FDA 510(k) K921922 Active Cleared 8 Jul 1992

See all devices from Ideal Medical, Inc. →