510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K844292Substantially Equivalent

Medi-Tech Dilatation Catheters

Medi-Tech, Inc., Watertown MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K844292 is the FDA 510(k) clearance record for MEDI-TECH DILATATION CATHETERS, a class I device, cleared for Medi-Tech, Inc. on under FDA product code LCN (Scraper, Tongue). FDA records list 36 510(k) clearances for Medi-Tech, Inc., from to . As of , FDA records show no recalls naming K844292.

Clearance record

Decision date
Received
(18 days to decision)
Product code
LCN Scraper, Tongue
Regulation
21 CFR 872.6855
Device class
Class I
Review panel
Dental
Applicant
Medi-Tech, Inc. 480 Plesant St., Watertown MA
Third party review
No

Clearances, product code LCN

Trailing 12 months

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

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