510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K962969Substantially Equivalent

Medical Device Technologies, Inc.ultra

Medical Device Technologies, Inc., Gainsville FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K962969 is the FDA 510(k) clearance record for MEDICAL DEVICE TECHNOLOGIES, INC.ULTRA, a class II device, cleared for Medical Device Technologies, Inc. on under FDA product code KNW (Instrument, Biopsy). FDA records list 46 510(k) clearances for Medical Device Technologies, Inc., from to . As of , FDA records show no recalls naming K962969.

Clearance record

Decision date
Received
(128 days to decision)
Product code
KNW Instrument, Biopsy
Regulation
21 CFR 876.1075
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Medical Device Technologies, Inc. 4445 SW 35th Ter., Gainsville FL
510(k) summary
Summary
Third party review
No

Clearances, product code KNW

Trailing 12 months
8 clearances under product code KNW in the twelve months to October 2026, August 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code KNW, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20261
April 20260
May 20261
June 20260
July 20260
August 20264
September 20260
October 20260