Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Siemens Life Support Systems — Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
123 daysmedian FDA review time
301 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K902859 | SERVO VENTILATOR 300 | Siemens Life Support Systems | 1991-04-26 | 301 | 3 |
| K903991 | PCM ANESTHESIA | Siemens Life Support Systems | 1991-02-25 | 180 | 0 |
| K901474 | ANESTHESIA WORKSTATION | Siemens Life Support Systems | 1990-04-10 | 14 | 0 |
| K893786 | SERVO ANESTHESIA CIRCLE 985 | Siemens Life Support Systems | 1989-09-22 | 123 | 0 |
| K890932 | CAV 3.0C SOFTWARE PROGRAM | Siemens Life Support Systems | 1989-06-12 | 108 | 0 |
| K890921 | DATA EXCHANGE SYSTEM, MODEL 24 | Siemens Life Support Systems | 1989-06-08 | 104 | 0 |
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