Nordiclab Intl.: FDA filings under this applicant name
FDA lists 8 510(k) clearances under the applicant name “Nordiclab Intl.” (first 1979, latest 1980), across 8 product codes in 2 review panels. Median 510(k) review time under this name: 23 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
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 |
|---|---|---|---|
| CDZ | Radioimmunoassay, Testosterones And Dihydrotestosterone | 1 | 1 |
| CGI | Radioimmunoassay, Estriol | 1 | 1 |
| CHP | Radioimmunoassay, Estradiol | 1 | 1 |
| DBF | Ferritin, Antigen, Antiserum, Control | 1 | 1 |
| JFH | Acid Phosphatase (Prostatic), Tartrate Inhibited | 1 | 1 |
| JLS | Radioimmunoassay, Progesterone | 1 | 1 |
| JMF | Radioimmunoassay, Human Placental Lactogen | 1 | 1 |
| JMG | Radioimmunoassay (Two-Site Solid Phase), Ferritin | 1 | 1 |
Review panels
- Clinical Chemistry (7)
- Immunology (1)
Most recent Nordiclab Intl. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K801988 | NORDICLAB PROSTATIC ACID PHOSPHATASE RIA | JFH | 1980-09-26 | 38 |
| K801989 | NORDICLAB FERRITIN IRMA TEST | DBF | 1980-09-16 | 28 |
| K800922 | NORDICLAB PROGESTERONE RIA TEST | JLS | 1980-05-14 | 23 |
| K800921 | NORDICLAB TESTOSTERONE RIA TEST | CDZ | 1980-05-14 | 23 |
| K800920 | NORDICLAB ESTRADIOL RIA TEST | CHP | 1980-05-14 | 23 |
| K792189 | NORDICLAB TOTAL ESTRIOL RIA TEST | CGI | 1979-11-13 | 13 |
| K782157 | IRMA TEST, NORDICLAB FERRITIN | JMG | 1979-01-17 | 26 |
| K782099 | RIA TEST, NORDICALB HPL | JMF | 1979-01-10 | 23 |
Recalls
openFDA lists no recalls under a recalling firm named Nordiclab Intl..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Frequently asked questions
How many FDA 510(k) clearances are listed under Nordiclab Intl.?
FDA lists 8 510(k) clearances under the applicant name “Nordiclab Intl.” (first 1979, latest 1980), across 8 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Nordiclab Intl.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Nordiclab Intl. is 23 days.
Which FDA product codes appear under Nordiclab Intl.?
The most frequent FDA product codes under this applicant name are CDZ (Radioimmunoassay, Testosterones And Dihydrotestosterone, 1); CGI (Radioimmunoassay, Estriol, 1); CHP (Radioimmunoassay, Estradiol, 1).
Next steps
- See all 8 Nordiclab Intl. clearances with predicates and recalls
- Run predicate analysis for product code CDZ, Nordiclab Intl.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.