510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K000620Substantially Equivalent

Pbn Fallopian Tube Catheter System

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

K000620 is the FDA 510(k) clearance record for PBN FALLOPIAN TUBE CATHETER SYSTEM, a class II device, cleared for Medical Device Technologies, Inc. on under FDA product code MDG (System, Intrafallopian Cannula). FDA records list 46 510(k) clearances for Medical Device Technologies, Inc., from to . As of , FDA records show no recalls naming K000620.

Clearance record

Decision date
Received
(249 days to decision)
Product code
MDG System, Intrafallopian Cannula
Regulation
21 CFR 884.4530
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Medical Device Technologies, Inc. 3600 S.W 47th Ave., Gainesville FL
510(k) summary
Summary
Third party review
No

Clearances, product code MDG

Trailing 12 months

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

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