510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K894771Substantially Equivalent

Epilation Needle

Precision Electrolysis Needles, Inc., Riverside RI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K894771 is the FDA 510(k) clearance record for EPILATION NEEDLE, a class I device, cleared for Precision Electrolysis Needles, Inc. on under FDA product code KCW (Epilator, High Frequency, Needle-Type). FDA records list one 510(k) clearance for Precision Electrolysis Needles, Inc. As of , FDA records show no recalls naming K894771.

Clearance record

Decision date
Received
(26 days to decision)
Product code
KCW Epilator, High Frequency, Needle-Type
Regulation
21 CFR 878.5350
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Precision Electrolysis Needles, Inc. 49 Arnold St., Riverside RI
Third party review
No

Clearances, product code KCW

Trailing 12 months

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

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