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
K770600Substantially Equivalent

Oropharyngeal Suction Airway

W.H. Wall, D.D.S., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K770600 is the FDA 510(k) clearance record for OROPHARYNGEAL SUCTION AIRWAY, a class I device, cleared for W.H. Wall, D.D.S. on under FDA product code EBR (Unit, Suction Operatory). FDA records list one 510(k) clearance for W.H. Wall, D.D.S. As of , FDA records show no recalls naming K770600.

Clearance record

Decision date
Received
(10 days to decision)
Product code
EBR Unit, Suction Operatory
Regulation
21 CFR 872.6640
Device class
Class I
Review panel
Dental
Applicant
W.H. Wall, D.D.S. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EBR

Trailing 12 months

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

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