510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K912767Substantially Equivalent

Fiber Optic Univeral Cables, Scope Adap., Lt.sourc

Microaire Advanced Surgical Products, Valencia CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K912767 is the FDA 510(k) clearance record for FIBER OPTIC UNIVERAL CABLES, SCOPE ADAP., LT.SOURC, a class I device, cleared for Microaire Advanced Surgical Products on under FDA product code EQH (Source, Carrier, Fiberoptic Light). FDA records list 2 510(k) clearances for Microaire Advanced Surgical Products, from to . As of , FDA records show no recalls naming K912767.

Clearance record

Decision date
Received
(50 days to decision)
Product code
EQH Source, Carrier, Fiberoptic Light
Regulation
21 CFR 874.4350
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Microaire Advanced Surgical Products 24907 Ave. Tibbetts, Valencia CA
510(k) summary
Statement
Third party review
No

Clearances, product code EQH

Trailing 12 months

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

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