510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K002971Substantially Equivalent

Mtg - Minitub Heated Stage Systems

Zander Medical Supplies, Inc., Vero Beach FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002971 is the FDA 510(k) clearance record for MTG - MINITUB HEATED STAGE SYSTEMS, a class II device, cleared for Zander Medical Supplies, Inc. on under FDA product code MQG (Accessory, Assisted Reproduction). FDA records list 5 510(k) clearances for Zander Medical Supplies, Inc., from to . As of , FDA records show no recalls naming K002971.

Clearance record

Decision date
Received
(84 days to decision)
Product code
MQG Accessory, Assisted Reproduction
Regulation
21 CFR 884.6120
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Zander Medical Supplies, Inc. 755 8th Ct., Suite #4, Vero Beach FL
510(k) summary
Summary
Third party review
No

Clearances, product code MQG

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