Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Chase Medical, Inc. · Predicate Candidate Screening

27 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

123 daysmedian FDA review time
190 days90th percentile
27clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K032531CHASE CARDIAC ANALYSIS SYSTEMChase Medical, Inc.2004-02-021710
K022093CHASE CARDIOVASCULAR PATCH KITChase Medical, Inc.2002-09-20850
K021129CHARE CARIOVASCULAR PATCHChase Medical, Inc.2002-06-03560
K020233CHASE CARDIOVASCULAR PATCH KITChase Medical, Inc.2002-03-14500
K020132CHASE CARDIOVASCULAR PATCH KITChase Medical, Inc.2002-02-26420
K012248CHASE CARDIOVASCULAR PATCHChase Medical, Inc.2001-08-10240
K003467CHASE CARDIOVASCULAR PATCHChase Medical, Inc.2001-01-29820
K001662CHASE CARDIOVASCULAR PATCHChase Medical, Inc.2000-08-02630
K972993CHASE FEMORAL ACCESS CANNULATION SETChase Medical, Inc.1998-03-312310
K974568CHASE ANASTOMOSIS VISUALIZATION DEVICEChase Medical, Inc.1998-01-06320
K971013CHASE TEMPERATURE PROBEChase Medical, Inc.1997-10-282220
K971023CHASE THORACIC CATHETERChase Medical, Inc.1997-09-081720
K972665CHASE BLOOD VESSEL SHUNTChase Medical, Inc.1997-08-22370
K971021CHASE PHRENIC NERVE PADChase Medical, Inc.1997-08-121450
K971019CHASE VESSEL CANNULAChase Medical, Inc.1997-07-211230
K964391CHASE LEFT VENT SAFETY VALVEChase Medical, Inc.1997-05-131900
K971041CHASE CORONARY OSTIAL PERFUSION CANNULAChase Medical, Inc.1997-05-13530
K970914CHASE AORTIC PERFUSION CANNULAChase Medical, Inc.1997-05-13620
K964393CHASE RETROGRADE CARDIOPLEGIA CANNULAChase Medical, Inc.1997-04-2317013
K971022CHASE SUCKERChase Medical, Inc.1997-04-17281
K964200CHASE MULTIPLE PERFUSION SETChase Medical, Inc.1997-04-161770
K964194CHASE CURVED LEFT HEART VENT CATHETERChase Medical, Inc.1997-04-161770
K964193CHASE AORTIC ARCH CANNULAChase Medical, Inc.1997-04-161770
K964199CHASE CORONARY SINUS PERFUSION CANNULAChase Medical, Inc.1997-03-191490
K964195CHASE TWO STAGE VENOUS RETURN CATHETERChase Medical, Inc.1997-03-191490
K964198CAHSE AORTIC ROOT CANNULAChase Medical, Inc.1997-03-191490
K964390CHASE VESSEL OCCLUDERChase Medical, Inc.1997-01-31880

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda