510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K012660Substantially Equivalent

Gimmi'alpha' Endoscopes & Accessories

Gimmi GmbH, Amsterdam, Nh, NL / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)

K012660 is the FDA 510(k) clearance record for GIMMI'ALPHA' ENDOSCOPES & ACCESSORIES, a class II device, cleared for Gimmi GmbH on under FDA product code FET (Endoscopic Video Imaging System/Component, Gastroenterology-Urology). FDA's definition for product code FET reads: "To allow for visualization of body cavities through an endoscope by projecting images to a monitor". FDA records list 3 510(k) clearances for Gimmi GmbH, from to . As of , FDA records show one recall naming K012660.

Clearance record

Decision date
Received
(129 days to decision)
Product code
FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Gimmi GmbH Amstel 320-I, Amsterdam, Nh, NL
510(k) summary
Summary
Third party review
No

Clearances, product code FET

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