FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ULTRASONIC HUMIDIFIER
K Number: K790966
·
Decision Jun 11, 1979
Classifications
1
FEI Numbers
119
Registration Numbers
119
Same Product Code
19
Applicant Total
2
Review Days
20
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Basic Information
- Device Name
- ULTRASONIC HUMIDIFIER
- K Number
- K790966
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.5460
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Hankscraft Div. of Gerber Products Co.
- Date Received
- May 22, 1979
- Decision Date
- June 11, 1979
- Product Code
- KFZ
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| KFZ | Humidifier, Non-Direct Patient Interface (Home-Use) | FDA class 1 | Anesthesiology |
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Other Clearances by Hankscraft Div. of Gerber Products Co.
| K Number | Device Name | ||
|---|---|---|---|
| K844013 | CARE ELECTRIC BREAST PUMP | Feb 15, 1985 | Substantially Equivalent |