Daavlin Co.
Bryan, OH, US
Daavlin Co. appears in FDA device records in Bryan, OH. FDA records list 5 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 5
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 5 510(k) clearances for Daavlin Co. between 1982 and 2007. The busiest year on record is 1982, with 1. The most recent is 2007, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1982 | 1 |
| 1983 | 1 |
| 1985 | 1 |
| 1993 | 1 |
| 2007 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K063621 | 3 SERIES PHOTOTHERAPY CABINET | FTC | Substantially Equivalent | |
| K930856 | PSORALITE | FTC | Substantially Equivalent | |
| K854498 | SPECTRA 724 | FTC | Substantially Equivalent | |
| K828654 | UVB CABINET OR GOEKERMAN CABINET, MODEL SPECTRA 305 | Substantially Equivalent | ||
| K827690 | SPECTRA MINI, ULTRAVIOLET EMITTER FOR DERMATOLOGICAL USE | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain