510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K121441Substantially Equivalent

Cautery; Low Temperature (Fineadjustable Fine Tip, Elongated Fine Tip, Micro Fine Tip)

Apyx Medical Corporation, Clearwater FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K121441 is the FDA 510(k) clearance record for CAUTERY; LOW TEMPERATURE (FINEADJUSTABLE FINE TIP, ELONGATED FINE TIP, MICRO FINE TIP), a class II device, cleared for Bovie Medical Corporation on under FDA product code HQP (Unit, Cautery, Thermal, Battery-Powered). FDA records list 75 510(k) clearances for Apyx Medical Corporation, from to . As of , FDA records show no recalls naming K121441.

Clearance record

Decision date
Received
(66 days to decision)
Product code
HQP Unit, Cautery, Thermal, Battery-Powered
Regulation
21 CFR 886.4115
Device class
Class II
Review panel
Ophthalmic
Applicant
Bovie Medical Corporation 5115 Ulmerton Rd., Clearwater FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HQP

Trailing 12 months

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

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