Panasonic Co. Div. Matsu Elec. Corp. America: FDA clearances and approvals
Panasonic Co. Div. Matsu Elec. Corp. America has 9 FDA 510(k) clearances (first 1982, latest 1986), across 3 product codes in 3 review panels. Median 510(k) review time: 45 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 |
|---|---|---|---|
| DXN | System, Measurement, Blood-Pressure, Non-Invasive | 5 | 5 |
| ESD | Hearing Aid, Air-Conduction, Prescription | 3 | 3 |
| FLL | Continuous Measurement Thermometer | 1 | 1 |
Review panels
Most recent Panasonic Co. Div. Matsu Elec. Corp. America 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K860634 | PANASONIC BLOOD PRESSURE METER, ZH-852AP, ZH-858PP | DXN | 1986-07-01 | 131 |
| K841103 | NONINVASIVE BLOOD PRESSURE MEASURE SYS | DXN | 1984-10-26 | 226 |
| K832076 | ELECTRONIC BLOOD PRESS. METER EN-212 | DXN | 1984-10-26 | 486 |
| K833510 | PANASONIC WH-50 HEARING AID | ESD | 1983-11-14 | 34 |
| K832075 | ELECTRONIC BLOOD PRESS. METER-ZH-820P | DXN | 1983-08-12 | 45 |
| K831151 | PANASONIC MODEL EW-213 | DXN | 1983-08-11 | 125 |
| K831150 | PANASONIC MODEL HV-5 | FLL | 1983-04-28 | 20 |
| K823285 | MODEL WHO1 HEARING AID | ESD | 1982-11-29 | 25 |
| K821972 | HEARING AID VARIOUS MODELS | ESD | 1982-07-20 | 18 |
Recalls
openFDA lists no recalls under a recalling firm named Panasonic Co. Div. Matsu Elec. Corp. America.
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 Panasonic Co. Div. Matsu Elec. Corp. America have?
Panasonic Co. Div. Matsu Elec. Corp. America has 9 FDA 510(k) clearances (first 1982, latest 1986), across 3 product codes in 3 review panels.
How long does FDA take to clear Panasonic Co. Div. Matsu Elec. Corp. America's 510(k)s?
The median time from FDA receipt to decision across Panasonic Co. Div. Matsu Elec. Corp. America's cleared 510(k)s is 45 days.
What devices does Panasonic Co. Div. Matsu Elec. Corp. America make?
Its most frequent FDA product codes are DXN (System, Measurement, Blood-Pressure, Non-Invasive, 5); ESD (Hearing Aid, Air-Conduction, Prescription, 3); FLL (Continuous Measurement Thermometer, 1).
Has Panasonic Co. Div. Matsu Elec. Corp. America had device recalls?
openFDA lists no recalls under a recalling firm name matching Panasonic Co. Div. Matsu Elec. Corp. America. Related entities may recall under other names.
Next steps
- See all 9 Panasonic Co. Div. Matsu Elec. Corp. America clearances with predicates and recalls
- Run predicate analysis for product code DXN, Panasonic Co. Div. Matsu Elec. Corp. America'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.