Atlas FDA

STOCKERT 1/4 BUBBLE SENSOR

FDA 510(k) clearance K925541 · decided 1993-02-02

Clearance details

K-number
K925541
Device name
STOCKERT 1/4 BUBBLE SENSOR
Applicant
Sorin Biomedica, Fiat, USA, Inc.
Decision
Substantially Equivalent
Date received
1992-11-03
Decision date
1993-02-02
Days to decision
91 days
Clearance type
Traditional
Product code
KRL
Device class
2
Regulation number
870.4205
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
STOCKERT AIR PURGE CONTROL SYSTEM MODEL 23-45-05 (K103469)Sorin Group Deutschland GmbH2011-01-18
CAPIOX BUBBLE TRAP WITH X-COATING (K090698)Terumo Cardiovascular Systems2009-06-08
EDAC QUANTIFIER (K071231)Luna Innovations, Inc.2007-05-17
AUTOMATIC TUBING CLAMP SYSTEM (ATC) (K961364)Rocky Mountain Research, Inc.1996-10-31
ELS AUTOMATIC TUBING CLAMP SYSTEM (K961598)Rocky Mountain Research, Inc.1996-10-29
SARNS ULTRASONIC AIR SENSOR (K940651)3M Health Care, Sarns1994-05-24
SARNS AIR DETECTION SYSTEM (K935977)3M Health Care, Sarns1994-02-04
STOCKERT CAPS1 CARDIOPLEGIC CONTROL MODULE (K925661)Sorin Biomedica, Fiat, USA, Inc.1993-05-18
CAPIOX(R) BUBBLE TRAP (K911632)Terumo Medical Corp.1991-07-09
CAPS LOW LEVEL DETECTOR & DETECTOR/BUBBLE MONITOR (K864619)Shiley, Inc.1987-02-03
COBE ACCESSORY INTERFACE MODULE (AIM) (K861860)Cobe Laboratories, Inc.1986-07-18
COBE AEPS (K842054)Cobe Laboratories, Inc.1984-08-02

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
AB-CORE K HEPATITIS B CORE ANTIGEN 125I (P850044/S003)Sorin Biomedica, Fiat, USA, Inc.1987-02-17
AB-CORE K HEPATITIS B CORE ANTIGEN 125I (P850044/S002)Sorin Biomedica, Fiat, USA, Inc.1986-10-31
AB-CORE K HEPATITIS B CORE ANTIGEN 125I (P850044/S001)Sorin Biomedica, Fiat, USA, Inc.1986-08-26