Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Zimmar Consulting , Ltd. — Predicate Candidate Screening
17 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
55 daysmedian FDA review time
90 days90th percentile
17clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K860322 | CLINISET INFUSION SET | Zimmar Consulting , Ltd. | 1986-04-07 | 68 | 0 |
| K843478 | PHARMA-PLAST URIDROP-URIDOME | Zimmar Consulting , Ltd. | 1984-12-05 | 90 | 0 |
| K843477 | PHARMA-PLAST RECTAL TIP | Zimmar Consulting , Ltd. | 1984-12-05 | 90 | 0 |
| K843468 | PHARMA-PLAST SUCTION SET TYPE YANKAUER | Zimmar Consulting , Ltd. | 1984-11-23 | 78 | 0 |
| K843466 | PHARMA-PLAST OXYGEN CATHETER | Zimmar Consulting , Ltd. | 1984-11-19 | 74 | 0 |
| K843469 | PHARMA-PLAST SUCTION TIP, TYPE ORTHOPAE- | Zimmar Consulting , Ltd. | 1984-11-19 | 74 | 0 |
| K843467 | PHARMA-PLAST NASAL OXYGEN CANNULA | Zimmar Consulting , Ltd. | 1984-11-19 | 74 | 0 |
| K843470 | PHARMA-PLAST CONNECTING TUBE TYPE SUCT- | Zimmar Consulting , Ltd. | 1984-11-16 | 71 | 0 |
| K843473 | PHARMA-PLAST INSULIN SYRINGE | Zimmar Consulting , Ltd. | 1984-10-31 | 55 | 0 |
| K843472 | PHARMA-PLAST SYRINGE WITH NEEDLE | Zimmar Consulting , Ltd. | 1984-10-31 | 55 | 0 |
| K843471 | PHARMA-PLAST SYRINGE | Zimmar Consulting , Ltd. | 1984-10-31 | 55 | 0 |
| K843475 | PHARMA-PLAST SINGLE USE OVERSHOES | Zimmar Consulting , Ltd. | 1984-10-31 | 55 | 0 |
| K843481 | PHARMA-PLAST CONNECTING TUBE TYPE URIN- | Zimmar Consulting , Ltd. | 1984-10-18 | 42 | 0 |
| K843479 | PHARMA-PLAST LEG BAG | Zimmar Consulting , Ltd. | 1984-10-11 | 35 | 0 |
| K843480 | PHARMA-PLAST URINARY DRAINAGE BAG 2000 | Zimmar Consulting , Ltd. | 1984-10-11 | 35 | 0 |
| K843476 | PHARMA-PLAST SMOOTH BORE CONNECTORS | Zimmar Consulting , Ltd. | 1984-09-24 | 18 | 0 |
| K843483 | PHARMA-PLAST PETRI DISH | Zimmar Consulting , Ltd. | 1984-09-21 | 15 | 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