510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K772171Substantially Equivalent

Ear Piercing Device

Robert C. Cameron, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K772171 is the FDA 510(k) clearance record for EAR PIERCING DEVICE, a class I device, cleared for Robert C. Cameron on under FDA product code JYS (Perforator, Ear-Lobe). FDA records list one 510(k) clearance for Robert C. Cameron. As of , FDA records show no recalls naming K772171.

Clearance record

Decision date
Received
(46 days to decision)
Product code
JYS Perforator, Ear-Lobe
Regulation
21 CFR 874.4420
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Robert C. Cameron 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JYS

Trailing 12 months

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

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