510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K810207Substantially Equivalent

Minor Surgery Light

Cavitron Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K810207 is the FDA 510(k) clearance record for MINOR SURGERY LIGHT, a class II device, cleared for Cavitron Corp. on under FDA product code GBC (Lamp, Surgical, Incandescent). FDA records list 32 510(k) clearances for Cavitron Corp., from to . As of , FDA records show no recalls naming K810207.

Clearance record

Decision date
Received
(18 days to decision)
Product code
GBC Lamp, Surgical, Incandescent
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Cavitron Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GBC

Trailing 12 months

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

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