510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K925367Substantially Equivalent

A-Dec 7284 Cuspidor, Cascade

A-dec, Inc., Newberg OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925367 is the FDA 510(k) clearance record for A-DEC 7284 CUSPIDOR, CASCADE, a class I device, cleared for A-Dec, Inc. on under FDA product code EBR (Unit, Suction Operatory). FDA records list 69 510(k) clearances for A-Dec, Inc., from to . As of , FDA records show no recalls naming K925367.

Clearance record

Decision date
Received
(537 days to decision)
Product code
EBR Unit, Suction Operatory
Regulation
21 CFR 872.6640
Device class
Class I
Review panel
Dental
Applicant
A-Dec, Inc. 2601 Crestview Dr., Newberg OR
510(k) summary
Statement
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