510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K830047Substantially Equivalent

Fiber Optic Laryngoscopes W/battery

Welch Allyn Inc, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830047 is the FDA 510(k) clearance record for FIBER OPTIC LARYNGOSCOPES W/BATTERY, a class I device, cleared for Welch Allyn, Inc. on under FDA product code CCW (Laryngoscope, Rigid). FDA records list 112 510(k) clearances for Welch Allyn, Inc., from to . As of , FDA records show no recalls naming K830047.

Clearance record

Decision date
Received
(8 days to decision)
Product code
CCW Laryngoscope, Rigid
Regulation
21 CFR 868.5540
Device class
Class I
Review panel
Anesthesiology
Applicant
Welch Allyn, Inc. 803 N. Front St. Suite 3, Mchenry IL
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