KCO
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Nasal Spray, Ent Delivery
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 874.5220
- Medical specialty
- Ear, Nose, Throat
- Flags
- GMP exempt
- Adverse events (MAUDE)
- 1994: 1 · 2005: 3
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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| Record | Firm | Date | Builder |
|---|---|---|---|
| SYN-O-SCOPE NASAL INHALER (K760674) | Mcdonald and Assoc., Inc. | 1977-03-10 | + Add |
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