The Perkin-Elmer Corp.: FDA filings under this applicant name
FDA lists 62 510(k) clearances under the applicant name “The Perkin-Elmer Corp.” (first 1976, latest 1994), across 17 product codes in 3 review panels. Median 510(k) review time under this name: 42 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 |
|---|---|---|---|
| JXR | Atomic Absorption Spectrophotometer, General Use | 17 | 17 |
| JJQ | Colorimeter, Photometer, Spectrophotometer For Clinical Use | 5 | 5 |
| KHO | Fluorometer, For Clinical Use | 5 | 5 |
| KZQ | Chromatography(Gas), Clinical Use | 5 | 5 |
| KZR | Chromatography (Liquid, Gel), Clinical Use | 5 | 5 |
| LDM | Instrumentation, High Pressure Liquid Chromatography | 5 | 5 |
| CCK | Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase | 3 | 3 |
| KIE | Apparatus, High Pressure Liquid Chromatography | 3 | 3 |
| DOP | Mass Spectrometer, Clinical Use | 2 | 2 |
| BXP | Transducer, Gas Flow | 1 | 1 |
Plus 7 more product codes.
Review panels
- Clinical Toxicology (38)
- Clinical Chemistry (12)
- Anesthesiology (7)
Most recent The Perkin-Elmer Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K935666 | PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP | KIE | 1994-04-26 | 151 |
| K900828 | PERKIN-ELMER AA 3100 ATOMIC ABSORPTION SPECTRO. | JXR | 1990-04-09 | 47 |
| K884864 | PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION SPECTRO | JJQ | 1989-02-10 | 80 |
| K884886 | MODEL 250 LIQUID CHROMOTAGRAPHY PUMP | LDM | 1989-02-02 | 72 |
| K872737 | PERKIN-ELMER LC235 DIODE ARRAY DETECTOR | — | 1987-09-18 | 71 |
| K872464 | ION TRAP DETECTOR (ITD) | DOP | 1987-08-11 | 49 |
| K871550 | PFI-20 POLARIZING FLUORIMETER | KHO | 1987-07-01 | 70 |
| K872122 | 8000 SERIES GAS CHROMATOGRAPHS | KZQ | 1987-06-17 | 15 |
| K870661 | LIFEWATCH PLUS | BZQ | 1987-03-09 | 18 |
| K862605 | MODULAR MASS SPECTROMETER (M.S.) | CCK | 1986-08-13 | 36 |
52 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named The Perkin-Elmer Corp..
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 The Perkin-Elmer Corp.?
FDA lists 62 510(k) clearances under the applicant name “The Perkin-Elmer Corp.” (first 1976, latest 1994), across 17 product codes in 3 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 The Perkin-Elmer Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name The Perkin-Elmer Corp. is 42 days.
Which FDA product codes appear under The Perkin-Elmer Corp.?
The most frequent FDA product codes under this applicant name are JXR (Atomic Absorption Spectrophotometer, General Use, 17); JJQ (Colorimeter, Photometer, Spectrophotometer For Clinical Use, 5); KHO (Fluorometer, For Clinical Use, 5).
Next steps
- See all 62 The Perkin-Elmer Corp. clearances with predicates and recalls
- Run predicate analysis for product code JXR, The Perkin-Elmer Corp.'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.