Metatech Corp.
Bonita Springs, FL, US
Metatech Corp. appears in FDA device records in Bonita Springs, FL. FDA records list 16 510(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
- 16
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 16 510(k) clearances for Metatech Corp. between 1985 and 2004. The busiest year on record is 1988, with 8. The most recent is 2004, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 1 |
| 1988 | 8 |
| 1989 | 1 |
| 1990 | 1 |
| 1992 | 1 |
| 1993 | 1 |
| 2002 | 1 |
| 2003 | 1 |
| 2004 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K033077 | EASYTEM DUO, FOREHEAD/EAR THERMOMETER, MODEL BT-021 | FLL | Substantially Equivalent | |
| K033082 | 9 SECOND DIGITAL THERMOMETER, MODEL BT-S09 | FLL | Substantially Equivalent | |
| K020520 | EASYTEM EAR THERMOMETER, MODEL BT-020 | FLL | Substantially Equivalent | |
| K924314 | MOBILE STANDING FRAME | IPL | Substantially Equivalent | |
| K915370 | COPPER VAPOR LASER SYSTEM | GEX | Substantially Equivalent | |
| K903883 | VASCULASE(R) COPPER VAPOR LASER SYST, PIGMENT LES | GEX | Substantially Equivalent | |
| K890865 | HEXASCAN SCANNER HANDPIECE | GEX | Substantially Equivalent | |
| K883541 | METALASER VASCULASE | GEX | Substantially Equivalent | |
| K883881 | MODIFIED MODEL 2001 FIBER OPTICS CATHETER | GWM | Substantially Equivalent | |
| K883518 | EVENT MARKER & A SECOND PRESSURE TREND OUTPUT | GWM | Substantially Equivalent | |
| K882552 | METATECH ROBINSON BOLT ACCESSORY | GWM | Substantially Equivalent | |
| K882367 | METATECH MICROCLIP APPLICATOR | DWS | Substantially Equivalent | |
| K882286 | EXPANSION COUPLER & MANUAL DRILL AS ACCESSORY SET | GWM | Substantially Equivalent | |
| K881447 | METATECH METAL MICROCLIP | DXC | Substantially Equivalent | |
| K880154 | METATECH INTRACRANIAL PRESSURE MONITORING SYSTEM | GWM | Substantially Equivalent | |
| K850538 | BED SENTRY, MODEL 50U | KPN | 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