LQM
7 FDA 510(k) clearances · Product code
119 daysmedian time to decision
272 days90th percentile
7clearances measured
FDA profile
- Official device name
- Gram Negative Identification Panel
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.2660
- Medical specialty
- Microbiology
- Adverse events (MAUDE)
- 2017: 77 · 2018: 88 · 2019: 12 · 2023: 30 · 2024: 34 · 2026: 35
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| ROCHE OXI/FERM II (K923313) | Roche Diagnostic Systems, Inc. | 1993-04-05 |
| VITEK RAPID CALL-GRAM NEGATIV IDENT CARD (K925915) | Biomerieux Vitek, Inc. | 1993-03-23 |
| SCEPTOR IDENTIFICATION SYSTEM (K912897) | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1991-10-28 |
| VITEK GRAM NEGATIVE IDENTIFICATION CARD, MODIFIED (K911429) | Vitek Systems, Inc. | 1991-06-24 |
| SENSITITRE AUTO ID PLATE AP80 (K890057) | Radiometer America, Inc. | 1989-06-09 |
| GRAM NEGATIVE FLUORESCENT IDENTIFICATION PANEL (K862642) | American Micro Scan | 1986-09-11 |
| PASCO GRAM NEGATIVE IDENTIFICATION SYSTEM (K851528) | Pasco Laboratories, Inc. | 1985-07-15 |
Track LQM automatically
Every clearance here is in the API, with alerts when new ones post.