510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K925078Substantially Equivalent

Spectradop

Bennett and Assoc., Inc., Cambridge OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925078 is the FDA 510(k) clearance record for SPECTRADOP, a class II device, cleared for Bennett and Assoc., Inc. on under FDA product code JOP (Transducer, Ultrasonic). FDA records list one 510(k) clearance for Bennett and Assoc., Inc. As of , FDA records show no recalls naming K925078.

Clearance record

Decision date
Received
(1,013 days to decision)
Product code
JOP Transducer, Ultrasonic
Regulation
21 CFR 870.2880
Device class
Class II
Review panel
Cardiovascular
Applicant
Bennett and Assoc., Inc. 67079 Read Rd., Cambridge OH
510(k) summary
Statement
Third party review
No

Clearances, product code JOP

Trailing 12 months

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

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