FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
HSC UNIT ROD
K Number: K871870
·
Decision Jul 21, 1987
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
6
Review Days
69
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Basic Information
- Device Name
- HSC UNIT ROD
- K Number
- K871870
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3050
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Applicant
- Research Development Corp.
- Date Received
- May 13, 1987
- Decision Date
- July 21, 1987
- Product Code
- KWP
- Advisory Committee
- Orthopedic
- Review Advisory Committee
- OR
- 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 |
|---|---|---|---|
| KWP | Appliance, Fixation, Spinal Interlaminal | FDA class 2 | Orthopedic |
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Other Clearances by Research Development Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K791730 | RING-ORIFICE, TURBULENT FLOW PNEUMOT | Nov 16, 1979 | Substantially Equivalent |
| K771407 | LUNG VOLUME & PRESSURE MONITOR | Aug 4, 1977 | Substantially Equivalent |
| K771019 | LUNG-MECHANICS MONITOR | Jun 14, 1977 | Substantially Equivalent |
| K770785 | MONITOR, RESPIRATORY, TWO-GAS, RDC | May 20, 1977 | Substantially Equivalent |
| K770061 | VO RESPIRATORY PNEUMOTACHOGRAPH | Jan 14, 1977 | Substantially Equivalent |