510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K900894Substantially Equivalent

Medilase Series 2100 Endoscope

Medical Laser, Inc., Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900894 is the FDA 510(k) clearance record for MEDILASE SERIES 2100 ENDOSCOPE, a class II device, cleared for Medical Laser, Inc. on under FDA product code GCQ (Endoscope, Flexible). FDA records list 8 510(k) clearances for Medical Laser, Inc., from to . As of , FDA records show no recalls naming K900894.

Clearance record

Decision date
Received
(115 days to decision)
Product code
GCQ Endoscope, Flexible
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Medical Laser, Inc. 2605 Fernbrook Ln., Minneapolis MN
Third party review
No

Clearances, product code GCQ

Trailing 12 months

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

FDA records show no clearances under product code GCQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GCQ, 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