510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K920580Substantially Equivalent

Transducer, Pressure, Catheter Tip

Greatbatch Medical, Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K920580 is the FDA 510(k) clearance record for TRANSDUCER, PRESSURE, CATHETER TIP, a class II device, cleared for Medamicus, Inc. on under FDA product code DXO (Transducer, Pressure, Catheter Tip). FDA records list 25 510(k) clearances for Greatbatch Medical, from to . As of , FDA records show no recalls naming K920580.

Clearance record

Decision date
Received
(332 days to decision)
Product code
DXO Transducer, Pressure, Catheter Tip
Regulation
21 CFR 870.2870
Device class
Class II
Review panel
Cardiovascular
Applicant
Medamicus, Inc. 15301 Hwy. 55 W., Minneapolis MN
510(k) summary
Summary
Third party review
No

Clearances, product code DXO

Trailing 12 months
1 clearance under product code DXO in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DXO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260