510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K890566Substantially Equivalent

Berman Type Airway #59422-59429 Various Sizes

Medi-Source, Inc., Syosset NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K890566 is the FDA 510(k) clearance record for BERMAN TYPE AIRWAY #59422-59429 VARIOUS SIZES, a class I device, cleared for Medi-Source, Inc. on under FDA product code CAE (Airway, Oropharyngeal, Anesthesiology). FDA records list 4 510(k) clearances for Medi-Source, Inc., from to . As of , FDA records show no recalls naming K890566.

Clearance record

Decision date
Received
(37 days to decision)
Product code
CAE Airway, Oropharyngeal, Anesthesiology
Regulation
21 CFR 868.5110
Device class
Class I
Review panel
Anesthesiology
Applicant
Medi-Source, Inc. 50 Gordon Dr., Syosset NY
Third party review
No

Clearances, product code CAE

Trailing 12 months

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

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