DEVILBISS MODEL 6300D
FDA 510(k) clearance K896090 · decided 1989-11-30
Clearance details
- K-number
- K896090
- Device name
- DEVILBISS MODEL 6300D
- Applicant
- Devilbiss Health Care, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1989-10-19
- Decision date
- 1989-11-30
- Days to decision
- 42 days
- Clearance type
- Traditional
- Product code
- EPN
- Device class
- 1
- Regulation number
- 874.5220
- Medical specialty
- Ear, Nose, Throat
- Advisory committee
- Ear, Nose, Throat
- Location
- Somerset, PA, 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 |
|---|---|---|
| NEBULIZER, MEDICINAL (K802430) | Dhd Medical Products Div. Diemolding Corp. | 1980-10-23 |
Recalls involving this device
No recalls on record reference this clearance.