510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K911756Substantially Equivalent

Posterior Nasal Epistaxis Instruments

Richard Wolf Medical Instruments Corp., Rosemont IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K911756 is the FDA 510(k) clearance record for POSTERIOR NASAL EPISTAXIS INSTRUMENTS, a class I device, cleared for Richard Wolf Medical Instruments Corp. on under FDA product code ECB (Unit, Syringe, Air And/Or Water). FDA records list 153 510(k) clearances for Richard Wolf Medical Instruments Corp., from to . As of , FDA records show no recalls naming K911756.

Clearance record

Decision date
Received
(189 days to decision)
Product code
ECB Unit, Syringe, Air And/Or Water
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Applicant
Richard Wolf Medical Instruments Corp. 7046 Lyndon Ave., Rosemont IL
510(k) summary
Statement
Third party review
No

Clearances, product code ECB

Trailing 12 months

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

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