FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
MICRO-STRAIGHT POSTURE TRAINING DEVICE
K Number: K884976
·
Decision Jun 9, 1989
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
4
Applicant Total
1
Review Days
191
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Basic Information
- Device Name
- MICRO-STRAIGHT POSTURE TRAINING DEVICE
- K Number
- K884976
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Applicant
- Mcdowell Ent., Inc.
- Date Received
- November 30, 1988
- Decision Date
- June 9, 1989
- Product Code
- LZW
- Advisory Committee
- Unknown
- 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 |
|---|---|---|---|
| LZW | Monitor, Spine Curvature | FDA unclassified | Unknown |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (LZW), ordered by most recent decision date.
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