Microquartz Medical, Inc.
Phoenix, AZ, US
Microquartz Medical, Inc. appears in FDA device records in Phoenix, AZ. FDA records list 6 510(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
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for Microquartz Medical, Inc. between 1995 and 1996. The busiest year on record is 1995, with 4. The most recent is 1996, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1995 | 4 |
| 1996 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K955861 | MICROQUARTZ MEDICAL TYPE B SIDE-FIRING LASER FIBER | GEX | Substantially Equivalent | |
| K954904 | MICROQUARTZ MEDICAL GENERAL SHAPE LASER FIBER | GEX | Substantially Equivalent | |
| K953065 | ULTRABRIGHT (MICROQUARTZ MEDICAL SIDE-FIRING LASER FIBER) | GEX | Substantially Equivalent | |
| K953174 | MICROQUATZ MEDICAL LINEAR MODULATOR ACCESSORY | GEX | Substantially Equivalent | |
| K952974 | QUADRALASE (MICROQUARTZ MEDICAL ADJUSTABLE SIDE-FIRING LASER FIBER) | GEX | Substantially Equivalent | |
| K950710 | MICROQUARTZ MEDICAL SIDE-FIRING LASER FIBER | GEX | 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