510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K942544Substantially Equivalent

Gip/medi-Globe Mechanical Lithotriptor and Baskets

Medi-Globe GmbH, Tempe AZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K942544 is the FDA 510(k) clearance record for GIP/MEDI-GLOBE MECHANICAL LITHOTRIPTOR AND BASKETS, a class II device, cleared for Medi-Globe Corp. on under FDA product code LQC (Lithotriptor, Biliary Mechanical). FDA records list 26 510(k) clearances for Medi-Globe Corp., from to . As of , FDA records show no recalls naming K942544.

Clearance record

Decision date
Received
(175 days to decision)
Product code
LQC Lithotriptor, Biliary Mechanical
Regulation
21 CFR 876.4500
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 LQC

Trailing 12 months

FDA records hold no clearances under product code LQC in the trailing twelve months.

FDA records show no clearances under product code LQC in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LQC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260