Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Compression Therapy Concepts, Inc. — Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
75 daysmedian FDA review time
156 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K112838 | VASOPRESS REPROCESSED DVT LEG / FOOT GARMENTS | Compression Therapy Concepts, Inc. | 2011-11-10 | 43 | 0 |
| K101915 | VASOPRESS SUPREME MINI MODEL VP500DM | Compression Therapy Concepts, Inc. | 2010-08-06 | 28 | 0 |
| K061814 | VASOPRESS DVT SYSTEM, MODEL VP500D | Compression Therapy Concepts, Inc. | 2006-11-30 | 156 | 0 |
| K061967 | SCD GARMENT, MODEL VP530 | Compression Therapy Concepts, Inc. | 2006-09-25 | 75 | 0 |
| K000147 | CTC DVT-1 CALF GARMENT, MODEL DVT-1 | Compression Therapy Concepts, Inc. | 2000-04-13 | 86 | 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