TAPE MEASURE
FDA 510(k) clearance K760521 · decided 1976-11-12
Clearance details
- K-number
- K760521
- Device name
- TAPE MEASURE
- Applicant
- Mcgaw Laboratories
- Decision
- Substantially Equivalent
- Date received
- 1976-08-26
- Decision date
- 1976-11-12
- Days to decision
- 78 days
- Clearance type
- Traditional
- Product code
- KTZ
- Device class
- 1
- Regulation number
- 888.4150
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| NK MEDICAL MICROMETER, MODEL MC001 (K921266) | Nk Biotechnical Engineering Co. | 1992-07-14 |
| SKYNDEX ELECTRONIC BODY FAT CALCULA (K841687) | Caldwell, Justiss & Co., Inc. | 1984-06-28 |
| SCOLIMETER (K831898) | Dr. Micheal A. Sabia | 1983-07-19 |
| A CALIPER (K820659) | Twin City Surgical, Inc. | 1982-03-19 |
| ISOROBIC SKINFOLD CALIPER (K810116) | Fitness Motivation Institute of America | 1981-02-04 |
| PARKE-DAVIS TOTAL KNEE PROSTHESIS (K800363) | Warner-Lambert Co. | 1980-03-10 |
Recalls involving this device
No recalls on record reference this clearance.