Atlas FDA

BAXTER HANDLE MODEL 1150

FDA 510(k) clearance K944214 · decided 1995-02-10

Clearance details

K-number
K944214
Device name
BAXTER HANDLE MODEL 1150
Applicant
Baxter Edwards
Decision
Substantially Equivalent
Date received
1994-08-29
Decision date
1995-02-10
Days to decision
165 days
Clearance type
Traditional
Product code
DTJ
Device class
1
Regulation number
870.3935
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Irvine, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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

RecordFirmDate
CARBOMEDICS HANDLE (K962154)Carbomedics, Inc.1996-08-27
CARBOMEDICS VALVE TESTER (K960169)Carbomedics, Inc.1996-04-15
CARBOMEDICS(R) PROSTHETIC HEART VALVE HOLDER HANDLE (K942736)Carbomedics, Inc.1994-07-06
EDWARDS-DUROMEDICS MITRAL VALVE ROTATOR (K880052)Baxter Healthcare Corp1988-04-01
IONESCU-SHILEY PERICARDIAL XENOGRAFT (ISU) (K871596)Shiley, Inc.1987-06-15
MODIFICATION OF CARPENTIER-EDWARDS BIOPROSTHESIS (K864155)American Edwards Laboratories1986-11-20
IONESCU-SHILEY VALVE HOLDER & HANDLE (K813276)Shiley, Inc.1981-12-10
DISPOSABLE HOLDER FOR HANCOCK MITRAL (K811235)Vascor, Inc.1981-05-13
DISPOSABLE HOLDER FOR HANCOCK AORTIC (K811236)Vascor, Inc.1981-05-13
INTEGRAL DISPOSABLE HOLDER CARPENTIER (K792034)Edwards Laboratories1979-12-07
DISPOSABLE HOLDER FOR BIOPROSTHESIS (K790022)Edwards Laboratories1979-01-15

Recalls involving this device

No recalls on record reference this clearance.