FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ATT-300
K Number: K944699
·
Decision May 26, 1995
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
70
Applicant Total
7
Review Days
245
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Basic Information
- Device Name
- ATT-300
- K Number
- K944699
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.5900
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Health Care Mfg., Inc.
- Date Received
- September 23, 1994
- Decision Date
- May 26, 1995
- Product Code
- ITH
- 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 |
|---|---|---|---|
| ITH | Equipment, Traction, Powered | FDA class 2 | Physical Medicine |
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Other Clearances by Health Care Mfg., Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K022667 | HCMI X-RAY | Oct 22, 2002 | Substantially Equivalent |
| K022737 | HCMI X-RAY HIGH REQUENCY CHIROPRACTIC RADIOGRAPHIC | Oct 22, 2002 | Substantially Equivalent |
| K952441 | LEGEND | Jun 19, 1995 | Substantially Equivalent |
| K951323 | VH-2000 | Jun 7, 1995 | Substantially Equivalent |
| K951382 | HLT 406 | Jun 1, 1995 | Substantially Equivalent |
| K944329 | BACK SPECIALIST | Mar 15, 1995 | Substantially Equivalent |