510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K981229Substantially Equivalent

Manan Manta Catheter Fixation Disk

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

K981229 is the FDA 510(k) clearance record for MANAN MANTA CATHETER FIXATION DISK, a class II device, cleared for Medical Device Technologies, Inc. on under FDA product code KNY (Accessories, Catheter, G-U). FDA records list 46 510(k) clearances for Medical Device Technologies, Inc., from to . As of , FDA records show no recalls naming K981229.

Clearance record

Decision date
Received
(19 days to decision)
Product code
KNY Accessories, Catheter, G-U
Regulation
21 CFR 876.5130
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 KNY

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