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
K161408Substantially Equivalent

Compass Cast and MAP

Centurion Medical Products, LP, Williamston MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K161408 is the FDA 510(k) clearance record for Compass Cast and MAP, a class II device, cleared for Centurion Medical Products Corporation on under FDA product code DRS (Transducer, Blood-Pressure, Extravascular). FDA records list 19 510(k) clearances for Centurion Medical Products Corporation, from to . As of , FDA records show no recalls naming K161408.

Clearance record

Decision date
Received
(186 days to decision)
Product code
DRS Transducer, Blood-Pressure, Extravascular
Regulation
21 CFR 870.2850
Device class
Class II
Review panel
Cardiovascular
Applicant
Centurion Medical Products Corporation 100 Centurion Way, Williamston MI
510(k) summary
Summary PDF
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