Beacon Laboratories, Inc.
Westminster, CO, US
Beacon Laboratories, Inc. appears in FDA device records in Westminster, CO. FDA records list 18 510(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
- 18
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 18 510(k) clearances for Beacon Laboratories, Inc. between 1989 and 1994. The busiest year on record is 1990, with 6. The most recent is 1994, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1989 | 3 |
| 1990 | 6 |
| 1991 | 2 |
| 1992 | 3 |
| 1993 | 3 |
| 1994 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K930243 | FLEXIBLE EXTENDER | GEI | Substantially Equivalent | |
| K930497 | ARGON HANDPIECES | GEI | Substantially Equivalent | |
| K925708 | DISPOSABLE ELECTROSURGERY BALL ELECTRODE | DWG | Substantially Equivalent | |
| K922289 | SESQUIPOLAR(TM) MIS ELECTRODE | GEI | Substantially Equivalent | |
| K925619 | DISPOSABLE HAND-SWITCHING ESU PENCIL | GEI | Substantially Equivalent | |
| K915788 | MIS ELECTROSURGICAL ELECTRODES | GEI | Substantially Equivalent | |
| K920100 | GSU HANDPIECE ADAPTER | HAM | Substantially Equivalent | |
| K913772 | PRESSURE GUARD | HIF | Substantially Equivalent | |
| K905752 | ARGON BEAM COMBO LAPAROSCOPIC ELECTRODE | GEI | Substantially Equivalent | |
| K904506 | ACTIVE ADAPTER | GEI | Substantially Equivalent | |
| K902996 | ARGON BEAM LAPAROSCOPIC ELECTRODE | GEI | Substantially Equivalent | |
| K903724 | BEAMER 1,2,4,6, AND 8 | GEI | Substantially Equivalent | |
| K902035 | FLEXIBLE EXTENDER | GEI | Substantially Equivalent | |
| K900767 | B-300 COMBINATION SWITCHING DISPOSABLE HANDPIECE | GEI | Substantially Equivalent | |
| K901248 | ABC HANDPIECE ADAPTER | HAM | Substantially Equivalent | |
| K894762 | B100 DISPOSABLE HANDPIECE | HAM | Substantially Equivalent | |
| K894663 | BEAMER ONE | HAM | Substantially Equivalent | |
| K894602 | B1 FOOTSWITCH (SINGLE PEDDLE), B2 (DOUBLE PEDDLE) | GEI | 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