AVL MODEL 912 CO-OXYLITE
FDA 510(k) clearance K895466 · decided 1989-11-06
Clearance details
- K-number
- K895466
- Device name
- AVL MODEL 912 CO-OXYLITE
- Applicant
- Avl Scientific Corp.
- Decision
- Substantially Equivalent
- Date received
- 1989-09-11
- Decision date
- 1989-11-06
- Days to decision
- 56 days
- Clearance type
- Traditional
- Product code
- GLY
- Device class
- 2
- Regulation number
- 864.7500
- Medical specialty
- Hematology
- Advisory committee
- Hematology
- Location
- Roswell, GA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| HEMONIR TM (K050014) | Nir Diagnostics, Inc. | 2005-05-05 |
| STAT PROFILE PHOX CO-OXIMETER ANALYZER, NOVA CO-OXIMETER CONTROLS, LEVELS 1 AND 2, NOVA CO-OXIMETER THB CALIBRATOR (K993104) | Nova Biomedical Corp. | 1999-12-02 |
| NOVA CO-OXIMETER ANALYZER (K955013) | Nova Biomedical Corp. | 1996-04-25 |
| MULTICHECK (K952725) | Radiometer America, Inc. | 1996-02-20 |
Recalls involving this device
No recalls on record reference this clearance.