FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TRANS 2000
K Number: K771018
·
Decision Jul 14, 1977
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
11
Applicant Total
5
Review Days
38
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Basic Information
- Device Name
- TRANS 2000
- K Number
- K771018
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.3690
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Hamilton Industries, Inc.
- Date Received
- June 6, 1977
- Decision Date
- July 14, 1977
- Product Code
- INK
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- PM
- 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 |
|---|---|---|---|
| INK | Stretcher, Wheeled, Powered | FDA class 2 | Physical Medicine |
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Other Clearances by Hamilton Industries, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K883680 | MEDALIST EXAMINATION TABLE | Oct 4, 1988 | Substantially Equivalent |
| K792001 | COMFICARE PAD (FOR SINGEL PT USE) | Oct 26, 1979 | Substantially Equivalent |
| K790871 | ENCLOSED CASE CART | May 14, 1979 | Substantially Equivalent |
| K770956 | PAS ANTI-EMBOLISM SYSTEM | Sep 12, 1977 | Substantially Equivalent |