Air Products & Chemicals, Inc.: FDA clearances and approvals
Air Products & Chemicals, Inc. has 2 FDA 510(k) clearances (first 1977, latest 1977), plus 1 PMA decision, across 3 product codes in 2 review panels. Median 510(k) review time: 25 days. It files with the SEC as Air Products & Chemicals, Inc. (APD).
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 |
|---|---|---|---|
| CAD | Vaporizer, Anesthesia, Non-Heated | 1 | 1 |
| CAI | Circuit, Breathing (W Connector, Adaptor, Y Piece) | 1 | 1 |
| LWL | Fluid, Intraocular | 1 | 0 |
Review panels
- Anesthesiology (2)
- Ophthalmic (1)
Most recent Air Products & Chemicals, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K771150 | COPPER KETTLE VAPORIZER PLUS | CAD | 1977-08-04 | 38 |
| K771134 | ANESTHESIA BREATHING CIRCUIT | CAI | 1977-07-05 | 12 |
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P910068 | PMA | VITREON(R) | 1997-09-30 |
Recalls
openFDA lists no recalls under a recalling firm named Air Products & Chemicals, Inc..
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.
SEC filings
Air Products & Chemicals, Inc. (APD): EDGAR filings, CIK 2969. Matched by exact company name.
Frequently asked questions
How many FDA 510(k) clearances does Air Products & Chemicals, Inc. have?
Air Products & Chemicals, Inc. has 2 FDA 510(k) clearances (first 1977, latest 1977), plus 1 PMA decision, across 3 product codes in 2 review panels.
How long does FDA take to clear Air Products & Chemicals, Inc.'s 510(k)s?
The median time from FDA receipt to decision across Air Products & Chemicals, Inc.'s cleared 510(k)s is 25 days.
What devices does Air Products & Chemicals, Inc. make?
Its most frequent FDA product codes are CAD (Vaporizer, Anesthesia, Non-Heated, 1); CAI (Circuit, Breathing (W Connector, Adaptor, Y Piece), 1); LWL (Fluid, Intraocular, 1).
Has Air Products & Chemicals, Inc. had device recalls?
openFDA lists no recalls under a recalling firm name matching Air Products & Chemicals, Inc. Related entities may recall under other names.
Next steps
- See all 2 Air Products & Chemicals, Inc. clearances with predicates and recalls
- Run predicate analysis for product code CAD, Air Products & Chemicals, Inc.'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.