510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K932738Substantially Equivalent

Kappler Pro/vent Boot

Kappler, Inc., Guntersville AL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932738 is the FDA 510(k) clearance record for KAPPLER PRO/VENT BOOT, a class I device, cleared for Kappler, Inc. on under FDA product code FXP (Cover, Shoe, Operating-Room). FDA records list 2 510(k) clearances for Kappler, Inc. As of , FDA records show no recalls naming K932738.

Clearance record

Decision date
Received
(295 days to decision)
Product code
FXP Cover, Shoe, Operating-Room
Regulation
21 CFR 878.4040
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Kappler, Inc. P.O. Box 218, Guntersville AL
510(k) summary
Summary
Third party review
No

Clearances, product code FXP

Trailing 12 months

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

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