510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902910Substantially Equivalent

Cytoaspirator

H & B Medical Technology, Inc., Norman OK / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902910 is the FDA 510(k) clearance record for CYTOASPIRATOR, a class II device, cleared for H & B Medical Technology, Inc. on under FDA product code FCK (Instrument, Biopsy, Suction). FDA records list one 510(k) clearance for H & B Medical Technology, Inc. As of , FDA records show no recalls naming K902910.

Clearance record

Decision date
Received
(198 days to decision)
Product code
FCK Instrument, Biopsy, Suction
Regulation
21 CFR 876.1075
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
H & B Medical Technology, Inc. 2001 Priestley Ave., Norman OK
Third party review
No

Clearances, product code FCK

Trailing 12 months

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

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