510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K921898Substantially Equivalent

Tad Model #9655

Loric Technology, Bellengham WA / Traditional, Substantially Equivalent

K921898 is the FDA 510(k) clearance record for TAD MODEL #9655, a class II device, cleared for Loric Technology on under FDA product code DRS (Transducer, Blood-Pressure, Extravascular). FDA records list one 510(k) clearance for Loric Technology. As of , FDA records show no recalls naming K921898.

Clearance record

Decision date
Received
(194 days to decision)
Product code
DRS Transducer, Blood-Pressure, Extravascular
Regulation
21 CFR 870.2850
Device class
Class II
Review panel
Cardiovascular
Applicant
Loric Technology 4760 Pacific Hgwy, Bellengham WA
510(k) summary
Statement
Third party review
No

Clearances, product code DRS

Trailing 12 months
1 clearance under product code DRS in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DRS, 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 20261
October 20260