Atlas FDA

VALVULOTOME

FDA 510(k) clearance K925283 · decided 1994-02-10

Clearance details

K-number
K925283
Device name
VALVULOTOME
Applicant
Intramed Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1992-10-20
Decision date
1994-02-10
Days to decision
478 days
Clearance type
Traditional
Product code
MGZ
Device class
2
Regulation number
870.4885
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
San Diego, CA, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Intramed Laboratories

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
LimFlow Vector (K260188)LimFlow, Inc.2026-03-18
Boomerang Valvulotome (BMGVT080); Boomerang Push Valvulotome (BMGPVT125) (K250105)Aveera Medical, Inc.2025-07-03
LimFlow Vector (K221902)LimFlow, Inc.2022-12-21
EZE SIT Valvulotome (K190267)Lemaitre Vascular2019-10-30
Antegrade LeMills Valvulotome (K142660)LeMaitre Vascular, Inc.2014-10-17
1.5MM HYDRO EXPANDABLE LEMAITRE VALVULOTOME (K140042)LeMaitre Vascular, Inc.2014-04-10
LEMILLS VALVULOTOME (K132047)LeMaitre Vascular, Inc.2013-11-05
EXPANDABLE LEMAITRE VALVULOTOME, OVER-THE-WIRE LEMAITRE VALVULOTOME (K132190)LeMaitre Vascular, Inc.2013-08-05
OVER-THE-WIRE EXPANDABLE LEMAITRE VALVULOTOME (K111884)LeMaitre Vascular, Inc.2011-07-29
VALVULOTOME BY KOVEN (K080178)Koven Technology, Inc.2008-07-28
VALVULOTOME, RETROGRADE : 03-7500- 03-7510, ANTEGRADE 03-7520 (K022823)Geister Medizin Technik GmbH2004-07-01
FOGARTY VALVULOTOME, MODEL 700091 (K001734)Edwards Lifesciences, LLC2001-03-26

Recalls involving this device

No recalls on record reference this clearance.