Atlas FDA

INTERFACE MODULE IDDD

FDA 510(k) clearance K992635 · decided 1999-12-20

Clearance details

K-number
K992635
Device name
INTERFACE MODULE IDDD
Applicant
Stoeckert Instrumente
Decision
Substantially Equivalent
Date received
1999-08-06
Decision date
1999-12-20
Days to decision
136 days
Clearance type
Special
Product code
KRI
Device class
1
Regulation number
870.4200
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
North Attleboro, MA, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Stoeckert Instrumente

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
3TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE (K020365)3t Medical Systems, LLC2002-05-03
STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS (K990512)Stoeckert Instrumente1999-11-23
AMMEX TUBING ORGANIZER (K934782)Ammex Cardiopulmonary Corp.1993-11-18
CARDIO2 CYCLE (K926233)Ergometrix, Inc.1993-06-04
TUBE GRIP (K922404)Georgia Medical Products, Inc.1992-11-23
NEWMARK(TM) CORONARY ARTERY BYPASS GRAFT MARKERS (K892856)Acacia Laboratories, Inc.1989-11-08
CARDIOTOMY RESERVOIR VALVE NO. CRV-30 OR PCRV-25 (K884893)American Omni Medical, Inc.1989-01-30
CARDIOPLEGIA OVERPRESSURE VALVE CPOP-350 & 700 (K884640)American Omni Medical, Inc.1989-01-24
HI-LO TEMP(R) MYOCARDIAL TEMPERATURE SENSOR (K874605)Mallinckrodt Critical Care1988-02-02
CPE 2000 CARDIO PULMONARY ERGOMETER (K874925)Medical Graphics Corp.1988-01-19
STOCKERT-SHILEY CAPS VENOUS OCCLUSION CLAMP (K864890)Shiley, Inc.1987-02-19
STOCKERT-SHILEY CAPS 4 CHANNEL TEMP. MONITOR 1 (K862510)Shiley, Inc.1986-07-17

Recalls involving this device

No recalls on record reference this clearance.