Laerdal California, Inc.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Laerdal California, Inc.” (first 1983, latest 1994), across 4 product codes in 3 review panels. Median 510(k) review time under this name: 96 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 |
|---|---|---|---|
| BTA | Pump, Portable, Aspiration (Manual Or Powered) | 2 | 2 |
| BSR | Stylet, Tracheal Tube | 1 | 1 |
| CBH | Device, Fixation, Tracheal Tube | 1 | 1 |
| IQK | Orthosis, Cervical | 1 | 1 |
Review panels
Most recent Laerdal California, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K941578 | STATVAC PORTABLE SUCTION UNIT | BTA | 1994-05-18 | 48 |
| K922842 | STYLET AND TRACHEAL LIGHTWAND (STL) | BSR | 1992-12-18 | 189 |
| K862875 | E-VAC(TM) | BTA | 1986-11-03 | 96 |
| K843790 | TRACHEAL TUBE FIXATION DEVICE | CBH | 1985-03-11 | 165 |
| K832990 | STIFNICK IMMOBILIZING COLLAR | IQK | 1983-11-07 | 67 |
Recalls
openFDA lists no recalls under a recalling firm named Laerdal California, Inc..
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.
- Laerdal Medical Corp. (11 510(k)s)
- Laerdal Medical AS (5 510(k)s)
- Laerdal Mfg. Corp. (5 510(k)s)
- Laerdal Medical A/S (4 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Laerdal California, Inc.?
FDA lists 5 510(k) clearances under the applicant name “Laerdal California, Inc.” (first 1983, latest 1994), across 4 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 Laerdal California, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Laerdal California, Inc. is 96 days.
Which FDA product codes appear under Laerdal California, Inc.?
The most frequent FDA product codes under this applicant name are BTA (Pump, Portable, Aspiration (Manual Or Powered), 2); BSR (Stylet, Tracheal Tube, 1); CBH (Device, Fixation, Tracheal Tube, 1).
Next steps
- See all 5 Laerdal California, Inc. clearances with predicates and recalls
- Run predicate analysis for product code BTA, Laerdal California, Inc.'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.