FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MODEL #510/515 GENERAL TRANSPORT STRETCHER
K Number: K895016
·
Decision Sep 11, 1989
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
34
Applicant Total
31
Review Days
34
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Basic Information
- Device Name
- MODEL #510/515 GENERAL TRANSPORT STRETCHER
- K Number
- K895016
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.3750
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Midmark Corp.
- Date Received
- August 8, 1989
- Decision Date
- September 11, 1989
- Product Code
- INW
- 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 |
|---|---|---|---|
| INW | Table, Mechanical | FDA class 1 | Physical Medicine |
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