FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
TAPE MEASURE
K Number: K760521
·
Decision Nov 12, 1976
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
6
Applicant Total
3
Review Days
78
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Basic Information
- Device Name
- TAPE MEASURE
- K Number
- K760521
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 888.4150
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Applicant
- Mcgaw Laboratories
- Date Received
- August 26, 1976
- Decision Date
- November 12, 1976
- Product Code
- KTZ
- 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 |
|---|---|---|---|
| KTZ | Caliper | FDA class 1 | Orthopedic |
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