VAPOCIDE
FDA 510(k) clearance K970726 · decided 1998-05-18
Clearance details
- K-number
- K970726
- Device name
- VAPOCIDE
- Applicant
- Cottrell, Ltd.
- Decision
- Substantially Equivalent
- Date received
- 1997-02-28
- Decision date
- 1998-05-18
- Days to decision
- 444 days
- Clearance type
- Traditional
- Product code
- MED
- Device class
- 2
- Regulation number
- 880.6885
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- North Attleboro, MA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.