Atlas FDA

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

Intelligent Medicine, Inc. · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K861598INTELLIGRAPH(TM) PROGRAMMERIntelligent Medicine, Inc.1986-07-24860
K861207INTELLIJECT INFUSION PUMPIntelligent Medicine, Inc.1986-06-30910
K861208INTELLIJECT MEDICATION SYRINGEIntelligent Medicine, Inc.1986-06-30910
K861209STREAM-SWITCH MANIFOLDIntelligent Medicine, Inc.1986-06-23840

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