510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K945901Substantially Equivalent

Direct View 2001 Fiberlight

Mercury Medical, Clearwater FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K945901 is the FDA 510(k) clearance record for DIRECT VIEW 2001 FIBERLIGHT, a class I device, cleared for Mercury Medical on under FDA product code CCW (Laryngoscope, Rigid). FDA records list 16 510(k) clearances for Mercury Medical, from to . As of , FDA records show no recalls naming K945901.

Clearance record

Decision date
Received
(25 days to decision)
Product code
CCW Laryngoscope, Rigid
Regulation
21 CFR 868.5540
Device class
Class I
Review panel
Anesthesiology
Applicant
Mercury Medical 11300-A 49th St. N., Clearwater FL
510(k) summary
Statement
Third party review
No

Clearances, product code CCW

Trailing 12 months

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

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