Teledyne Avionics Div. of Teledyne: FDA filings under this applicant name
FDA lists 13 510(k) clearances under the applicant name “Teledyne Avionics Div. of Teledyne” (first 1979, latest 1986), across 5 product codes in 2 review panels. Median 510(k) review time under this name: 46 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 |
|---|---|---|---|
| ETY | Tester, Auditory Impedance | 5 | 5 |
| EWO | Audiometer | 4 | 4 |
| BTY | Calculator, Predicted Values, Pulmonary Function | 2 | 2 |
| BZC | Calculator, Pulmonary Function Data | 1 | 1 |
| BZG | Spirometer, Diagnostic | 1 | 1 |
Review panels
Most recent Teledyne Avionics Div. of Teledyne 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K860262 | TA-6C - PART NUMBER SLZ 7520 | ETY | 1986-04-23 | 89 |
| K860522 | SPIROMETER, MODEL TS-1000, PART NO. SLZ7504 | BZG | 1986-03-03 | 20 |
| K855068 | SPIROMETER, MODEL TS-500 PART #SLZ7534 | BTY | 1986-02-05 | 49 |
| K855070 | SPIROMETER MODEL TS-200 SLZ 7541 | BZC | 1986-01-30 | 43 |
| K855069 | SPIROMETER TS-400 SLZ 7547 | BTY | 1986-01-30 | 43 |
| K854043 | AUTOMATIC IMPEDANCE AUDIOMETER, TA-7B | ETY | 1985-12-31 | 90 |
| K851015 | TA-20 AUTOMATIC INDUSTIRAL AUDIOMETER | EWO | 1985-06-04 | 84 |
| K850461 | AUTOMATIC IMPEDANCE METER TA-7A | ETY | 1985-03-25 | 47 |
| K844069 | TA-201 CLINICAL AUDIOMETER | EWO | 1984-12-03 | 46 |
| K811509 | AUTO-TYMPANIGRAPH (TA-5A) | ETY | 1981-06-16 | 20 |
3 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Teledyne Avionics Div. of Teledyne.
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.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Teledyne, Inc. (10 510(k)s)
- Teledyne Water Pik (9 510(k)s)
- Teledyne Getz (5 510(k)s)
- Teledyne Densco (4 510(k)s)
- Teledyne Analytical Instruments (3 510(k)s)
- Teledyne Brown Engineering (2 510(k)s)
- Teledyne Electronic Technologies (2 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Teledyne Avionics Div. of Teledyne?
FDA lists 13 510(k) clearances under the applicant name “Teledyne Avionics Div. of Teledyne” (first 1979, latest 1986), across 5 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 Teledyne Avionics Div. of Teledyne?
The median time from FDA receipt to decision across 510(k)s cleared under the name Teledyne Avionics Div. of Teledyne is 46 days.
Which FDA product codes appear under Teledyne Avionics Div. of Teledyne?
The most frequent FDA product codes under this applicant name are ETY (Tester, Auditory Impedance, 5); EWO (Audiometer, 4); BTY (Calculator, Predicted Values, Pulmonary Function, 2).
Next steps
- See all 13 Teledyne Avionics Div. of Teledyne clearances with predicates and recalls
- Run predicate analysis for product code ETY, Teledyne Avionics Div. of Teledyne'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.