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

Stoeckert Instrumente — Predicate Candidate Screening

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

187 daysmedian FDA review time
278 days90th percentile
13clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K002273STOCKERT A272 SERIES PEDIATRIC AORTIC CANNULAEStoeckert Instrumente2001-01-291870
K001961STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAEStoeckert Instrumente2001-01-252120
K002118STOCKERT COMPACT SYSTEM VERSION 2.0Stoeckert Instrumente2000-08-09270
K992635INTERFACE MODULE IDDDStoeckert Instrumente1999-12-201360
K990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSStoeckert Instrumente1999-11-232780
K982014STOCKERT COMPACT SYSTEMStoeckert Instrumente1998-09-04880
K972321S3 MAST PUMPStoeckert Instrumente1998-02-272490
K971520S3 CYCLIC RPM CONTROLStoeckert Instrumente1997-09-101380
K962320S3 CARDIOPLEGIA CONTROLStoeckert Instrumente1997-01-102070
K955152STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMStoeckert Instrumente1996-02-221010
K955038STOCKERT S3 DOUBLE HEAD PUMP MODULEStoeckert Instrumente1996-02-211100
K950990STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLEStoeckert Instrumente1996-01-193220
K812049STOCKERT CARDIAC PACING ELECTRODESStoeckert Instrumente1982-03-182400

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