Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K942005Substantially Equivalent

Gip/med-Globe Stone Extractor Baskets

Medi-Globe GmbH, Tempe AZ / Traditional, Substantially Equivalent

K942005 is the FDA 510(k) clearance record for GIP/MED-GLOBE STONE EXTRACTOR BASKETS, a class II device, cleared for Medi-Globe Corp. on under FDA product code LQR (Dislodger, Stone, Biliary). FDA records list 26 510(k) clearances for Medi-Globe Corp., from to . As of , FDA records show no recalls naming K942005.

Clearance record

Decision date
Received
(211 days to decision)
Product code
LQR Dislodger, Stone, Biliary
Regulation
21 CFR 876.5010
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Medi-Globe Corp. 6202 S. Maple Ave. # 131, Tempe AZ
510(k) summary
Summary
Third party review
No

Clearances, product code LQR

Trailing 12 months
1 clearance under product code LQR in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LQR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260