510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K770812Substantially Equivalent

Handles, Light, Surgical, Steoile

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

K770812 is the FDA 510(k) clearance record for HANDLES, LIGHT, SURGICAL, STEOILE, a class II device, cleared for Sybron Corp. on under FDA product code FQP (Lamp, Operating-Room). FDA records list 37 510(k) clearances for Sybron Corp., from to . As of , FDA records show no recalls naming K770812.

Clearance record

Decision date
Received
(20 days to decision)
Product code
FQP Lamp, Operating-Room
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Sybron Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FQP

Trailing 12 months

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

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