Morrison Medical Products: FDA clearances and approvals
Morrison Medical Products has 8 FDA 510(k) clearances (first 1996, latest 1996), across 1 product code in 1 review panel. Median 510(k) review time: 70 days.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| FMQ | Restraint, Protective | 8 | 8 |
Review panels
- General Hospital (8)
Most recent Morrison Medical Products 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K963387 | DELUXE LIMB RESTRAINT WITH DOUBLE D-RING AND STRAP DELUXE LIMB RESTRAINT WITH STRAP | FMQ | 1996-11-08 | 72 |
| K963374 | TORSO/WAIST RESTRAINT | FMQ | 1996-11-08 | 73 |
| K963370 | CINCH STRAP WITH BUCKLE | FMQ | 1996-11-08 | 73 |
| K963371 | BEST STRAP RESTRAINT | FMQ | 1996-11-07 | 72 |
| K963494 | MORRISON MEDICAL DISPOSABLE RESTRAINT STRAP | FMQ | 1996-11-06 | 64 |
| K963416 | ANKLE RESTRAINT SYSTEM | FMQ | 1996-11-06 | 68 |
| K963399 | MORRISON MEDICAL STRETCHER/COT AND BACKBOARD RESTRAINTS | FMQ | 1996-11-06 | 69 |
| K963419 | MORRISON MEDICAL WRIST RESTRAINT | FMQ | 1996-10-31 | 62 |
Recalls
openFDA lists no recalls under a recalling firm named Morrison Medical Products.
Recalling firms are matched to this company by name only (same normalization as the applicant), so related entities that recall under another name are not counted.
Frequently asked questions
How many FDA 510(k) clearances does Morrison Medical Products have?
Morrison Medical Products has 8 FDA 510(k) clearances (first 1996, latest 1996), across 1 product code in 1 review panel.
How long does FDA take to clear Morrison Medical Products's 510(k)s?
The median time from FDA receipt to decision across Morrison Medical Products's cleared 510(k)s is 70 days.
What devices does Morrison Medical Products make?
Its most frequent FDA product codes are FMQ (Restraint, Protective, 8).
Has Morrison Medical Products had device recalls?
openFDA lists no recalls under a recalling firm name matching Morrison Medical Products. Related entities may recall under other names.
Next steps
- See all 8 Morrison Medical Products clearances with predicates and recalls
- Run predicate analysis for product code FMQ, Morrison Medical Products's most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.